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United States Patent Application	20090133160
Kind Code	A1
Scott; Richard William ;   et al.	May 21, 2009

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Foreign Application Data

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Date	Code	Application Number
Oct 19, 2005	AU	2005905787
Nov 16, 2005	AU	2005906364

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Claims

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1. A construct comprising nucleic acid sequences encoding two or more oleosin repeat units.

2. A construct according to claim 1 wherein the oleosin repeat units are tandem repeats.

3. A construct according to claim 1 further comprising a nucleotide sequence encoding a linking sequence disposed between nucleic acids sequences encoding two of the oleosin repeat units.

4. A construct according to claim 3 wherein said linking sequences are selected to enable degradation, allow flexibility and/or induce a directional change between the oleosin repeat units.

5. A construct according to claim 3 wherein the linking sequences comprise a site for enzymatic cleavage.

6. A construct according to claim 1 further comprising one or more nucleic acid sequences encoding bioactive peptides.

7. A construct according to claim 1 wherein the construct comprises nucleic acids encoding between two and ten oleosin repeat units.

8. A construct according to claim 1 wherein the nucleic acid sequences encoding oleosin repeat units are from white clover or sesame seed or are a recombinant or synthetic version thereof.

9. A construct according to claim 8 wherein said nucleic acids sequences encoding oleosin repeat units are modified to enhance expression of said construct.

10. A construct according to claim 1 wherein the nucleic acids sequences encoding oleosin repeat units comprise a nucleotide sequence selected from the group consisting of sequences shown in FIGS. 13, 15, 17, 19, 21, 23, 25, 27, 31, 34, 70, 72-77 and 97-106 hereto, and functionally active fragments and variants thereof.

11. A construct according to claim 1 further comprising a nucleic acid sequence encoding a diacylglycerol acryltransferase or a functionally active fragment or variant thereof.

12. A cell in accordance with claim 13, wherein the cell is plant cell, and the plant cell is isolated or part of a plant, plant seed or other plant part.

13. An eukaryotic or prokaryotic cell comprising a construct comprising nucleic acid sequences encoding two or more oleosin repeat units.

14. A method according to claim 15, wherein the eukaryotic cell is a plant cell and is part of.

15. A method of producing repeat oleosins in a cell, said method comprising introducing into said cell a construct according to claim 1, and expressing the construct.

16. A method according to claim 15 wherein the cell is a prokaryotic cell.

17. A partially or substantially purified and/or recombinant polypeptide comprising two or more oleosin repeat units.

18. A polypeptide according to claim 17 produced by expression of a construct according to claim 1.

19. A polypeptide according to claim 17 wherein the oleosin repeat units are tandem repeats.

20. A polypeptide according to claim 17 further comprising linking sequences between two or more of the oleosin repeat units.

21. A polypeptide according to claim 17 further comprising one or more bioactive peptides.

22. A polypeptide according to claim 21 wherein said bioactive peptide is inserted at the N or C terminus of said oleosin repeat units or between two or more oleosin repeat units.

23. A polypeptide according to claim 17 comprising between two and ten oleosin repeat units.

24. A polypeptide according to claim 17 wherein the oleosin repeat units are from white clover or sesame seed or are a synthetic or recombinant version thereof.

25. A polypeptide according to claim 17 including an amino acid sequence selected from the group consisting of the sequences shown in FIGS. 69, 70, 78-83 and 107-116 hereto, and functionally active fragments and variants thereof.

26. A lipid encapsulated by a polypeptide according to claim 17.

27. (canceled)

28. A method according to claim 36 wherein the cell or organism is a plant, thereby altering emulsification properties, physiochemical properties or degree of biohydrogenation of said lipids.

29. A method according to claim 36, wherein the cell or organism is a plant, thereby altering stability of an oil body in a plant.

30. A method of altering biohydrogenation of a lipid, said method comprising encapsulating said lipid in a recombinant polypeptide comprising two or more oleosin repeat units.

31. A method according to claim 30, wherein the lipid is an unsaturated lipid and said unsaturated lipid into an oil body comprising the recombinant polypeptide.

32. A method of delivering a bioactive peptide, to animals including humans, said method comprising inserting said peptide at the N- or C-terminus of a series of two or more oleosin repeat units or between two or more oleosin repeat units to produce a recombinant polypeptide and administering said recombinant polypeptide to said animal.

33. A method of delivering compounds and/or organisms to animals including humans, said method comprising encapsulation said compound or organism in an oil body including two or more oleosin repeat units and administering said oil body to said animal.

34. A method of altering the emulsification properties of an oleosin, said method comprising recombinantly producing the oleosin with two or more oleosin repeat units.

35. A polypeptide according to claim 17, wherein the polypeptide is a recombinant oleosin having altered emulsification properties.

36. A method for modifying lipid metabolism or storage in a cell or organism, comprising introducing into said cell or organism a construct according to claim 1 and expressing the construct.

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Description

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[0001]The present invention relates to constructs including one or more nucleic acids encoding two or more oleosin repeat units, and methods of use thereof. The present invention also relates to recombinant polypeptides including two or more oleosin repeat units, and methods of use thereof.

Triacylglycerol

[0002]Most plants synthesise and store significant amounts of triacylglycerol (TAG) only in developing embryos and pollen cells where it is subsequently utilised to provide catabolizable energy during germination and pollen tube growth. Dicotyledonous plants can accumulate up to approximately 60% of their seed weight as TAG. Ordinarily, this level is considerably lower in the monocotyledonous seeds where the main form of energy storage is carbohydrates (e.g., starch).

[0003]The only committed step in TAG biosynthesis is the last one, i.e., the addition of a third fatty acid to an existing diacylglycerol, thus generating TAG. In plants this step is performed by one of three enzymes including: acyl CoA: diacylglycerol acyltransferase (DGAT1); an unrelated acyl CoA: diacylglycerol acyl transferase (DGAT2); and phospholipid: diacylglycerol acyltransferase (PDAT) (Bouvier-Nave et al., 2000; Dahlqvist et al., 2000; Lardizabal et al., 2001; Zou et al., 1999).

Oleosin

[0004]Oleosins are specific plant proteins usually found only in seeds and pollen. Their function is to stop oil bodies coalescing during seed and pollen dehiscence. In nature, TAG produced in seeds and pollen form micelles encapsulated by a spherical phospholipid monolayer and one or several species of oleosin proteins. Oil bodies in fruit tissues (such as olives and avocados) do not contain oleosins.

[0005]The physiochemical properties of the major oleosins is relatively conserved between plants and is characterised by the following: [0006]15-25 kDa protein corresponding to approximately 140-230 amino acid residues. [0007]The protein sequence can be divided almost equally along its length into 4 parts that correspond to a N-terminal hydrophilic region; two centre hydrophobic regions (joined by a proline knot or knob) and a C-terminal hydrophilic region. [0008]The topology of oleosin is attributed to its physiochemical properties, which includes a folded hydrophobic core flanked by hydrophilic domains (FIG. 1). This arrangement confers an amphipathic nature to oleosin resulting in the hydrophobic domain being embedded in the phospholipid monolayer (Tzen et al., 1992) while the flanking hydrophilic domains are exposed to the aqueous environment of the cytoplasm (FIG. 2).

Oil Bodies

[0009]An oil body that is produced in seed or pollen consists of a droplet of TAG surrounded by a monolayer of phospholipid where the hydrophobic acyl moieties of the phospholipids interact with the encapsulated TAG and the hydrophilic head groups face the cytoplasm. Oil bodies are naturally produced in the seeds and pollen of many plants. Oil bodies can also be generated artificially by combining oleosins, triacylglycerides and phospholipids (Peng et al., 2004).

[0010]The outside of the oil body is coated with oleosins which are orientated with their central hydrophobic amino acid domains protruding through the phospholipid monolayer and into the TAG core of the oil body (FIGS. 2-6).

[0011]The size of the oil body may be regulated by oleosin imparting a defined curvature; the curvature is dependent on the oleosin::oil ratio as well as the type of oleosin and oil.

Biohydrogenation

[0012]It has been demonstrated that the lipid profile of ruminant animal feed in turn influences the lipid profile of meat and dairy products (Demeyer and Doreau, 1999). Different plants have different lipid profiles; by selectively feeding animals only plants with the desired lipid profile it is possible to positively influence the lipid profile of downstream meat and dairy products. In ruminants the final lipid make up of the meat and milk is not only influenced by the dietary lipids but is also heavily influenced by biohydrogenation. Biohydrogenation is the hydrogenation of non-reduced compounds (such as unsaturated fats) by the biota present in the rumen.

Emulsions

[0013]Emulsions are produced when one or more liquids that are immiscible (usually due to different polarities and thus different hydrophobicities) in another liquid are uniformly suspended within that liquid, for example when oil droplets are dispersed uniformly in water or water droplets dispersed uniformly in oil. Generation of a relatively stable emulsion requires the use of an emulsifier, which lowers the interfacial tension between the liquids. The stability of an emulsion is generally a measure of what conditions and for how long the uniform dispersion persists. Emulsifiers are commonly used in the food and cosmetic industry; as such the emulsifiers need to have high emulsion stability as well as be safe for consumption and topical application.

[0014]It is an object of the present invention to overcome, or at least alleviate, one or more of the difficulties or deficiencies associated with the prior art.

[0015]In one aspect the present invention provides a construct including one or more nucleic acids encoding two or more oleosin repeat units. For expression in vegetative plant tissue preferably the construct further includes a nucleic acid encoding a diacylglycerol acryltransferase.

[0016]The term "oleosin" as used herein includes any functionally active plant oleosin, including functionally active fragments and variants thereof (e.g., L-oleosin, H-oleosin, steroleosin and caoleosin).

[0017]In a preferred embodiment, the oleosin repeat unit may be from white clover or sesame seed, or may be a synthetic or recombinant version of an oleosin repeat unit from white clover or sesame seed.

[0018]While Applicants have exemplified the invention using white clover and sesame seed oleosins, the invention is not limited thereto and any functionally active plant oleosin sequence may be used in the constructs of the present invention. The oleosin sequence may be naturally occurring, recombinant or synthetic.

[0019]By "repeat units" is meant multiple copies of nucleotide sequences encoding oleosin within a single polynucleotide, or multiple copies of amino acid sequences encoding oleosin within a single polypeptide, which may or may not contain intervening nucleotide or amino acid sequences. The repeat units may be tandem repeats. The repeat units may be homo- or hetero-repeats (homo or heteromeric).

[0020]The oleosin repeat units may be linked either directly, for example by direct fusion of the repeats, or by using linking sequences.

[0021]In a preferred embodiment of this aspect of the invention linker sequences may be included between the oleosin repeats to facilitate rotation of the oleosin hydrophilic domains relative to each other to form the correct topology. Such linker sequences also facilitate recombinatorial subcloning of sequences encoding desired peptides in between the oleosin repeats, and also facilitate chemical or enzymatic cleavage, for example to destroy the multimeric oleosin chain and/or release the desired peptide from the multimeric oleosin chain.

[0022]Thus, the construct may further include nucleotide sequences encoding linking sequences between two or more of the oleosin repeat units. The linking sequences may be short sequences, for example sequences that allow flexibility between the repeat units (act as a flexible hinge) or induce a directional change (act as a directional induction hinge) between the repeats, enable degradation between the oleosin repeat units, for example by peptidases, unrelated peptide sequences that may have bioactive properties, or sites for enzymatic cleavage and or subsequent fusion.

[0023]More particularly, the linking nucleotide sequence(s) between the oleosin repeat units may encode the native N- and C-termini of the respective repeats, sequences that code for comparatively short peptides that allow flexibility between the repeats, comparatively short peptides with amino acid residues that induce a directional change in the chain (for example proline), sequences that enable the future targeted cloning of additional sequences between the repeats, sequences that encode for specific targeted peptidase degradation, sequences that encode for bioactive peptides, and/or sequences encoding sites for specific enzymatic cleavage and subsequent fusion, e.g., modified self splicing intein and polymerisation cyclisation (Williams et al., 2005).

[0024]The multiple oleosin nucleotide sequences may code for the same oleosin peptide sequence or code for different oleosin peptide sequences. The multiple oleosin nucleotide sequences may code for the same oleosin peptide sequence but use alternate codons in the nucleotide sequence where applicable. This enables the construct to also be used in prokaryotic expression systems that are not non-recombinant minus (rec.sup.-). It also enables the use of oleosins that contain different affinities for the oil body.

[0025]In a particularly preferred embodiment of the present invention, the nucleic acid encoding an oleosin repeat unit includes a nucleotide sequence selected from the group consisting of sequences shown in FIGS. 13, 15, 17, 19, 21, 23, 25, 27, 31, 34, 70, 72-77 and 97-106 hereto, and functionally active fragments and variants thereof.

[0026]The construct of the present invention includes one or more nucleic acids encoding two or more oleosin repeats, preferably between two or three and twenty oleosin repeats, more preferably between two or three and ten oleosin repeats, most preferably between two or three and five or six oleosin repeats.

[0027]The diacylglycerol acyltransferase may be of any suitable type, including functionally active fragments and variants thereof. In a preferred form, the diacylglycerol acyltransferase is selected from the group consisting of DGAT1, DGAT2 and PDAT.

[0028]Nucleic acids according to the invention may be full-length genes or part thereof, and are also referred to as "nucleic acid fragments" and "nucleotide sequences" in this specification.

[0029]The nucleic acid may be of any suitable type and includes DNA (such as cDNA or genomic DNA) and RNA (such as mRNA) that is single- or double-stranded, optionally containing synthetic, non-natural or altered nucleotide bases, and combinations thereof.

[0030]By "functionally active" in respect of a nucleotide sequence is meant that the fragment or variant (such as an analogue, derivative or mutant) is capable of modifying lipids in a plant. Such variants include naturally occurring allelic variants and non-naturally occurring variants. Additions, deletions, substitutions and derivatizations of one or more of the nucleotides are contemplated so long as the modifications do not result in loss of functional activity of the fragment or variant. Preferably the functionally active fragment or variant has at least approximately 80% identity to the relevant part of the oleosin repeat sequences exemplified herein, more preferably at least approximately 90% identity, most preferably at least approximately 95% identity. Such functionally active variants and fragments include, for example, those having nucleic acid changes that result in conservative amino acid substitutions of one or more residues in the corresponding amino acid sequence. For example, the nucleic acid sequence may be modified to enhance expression without altering the amino acid sequence. Preferably the fragment has a size of at least 30 nucleotides, more preferably at least 45 nucleotides, most preferably at least 60 nucleotides.

[0031]By "functionally active" in the context of a polypeptide is meant that the fragment or variant has one or more of the biological properties of oleosin polypeptides. Additions, deletions, substitutions and derivatizations of one or more of the amino acids are contemplated so long as the modifications do not result in loss of functional activity of the fragment or variant. Preferably the functionally active fragment or variant has at least approximately 60% identity to the relevant part of the oleosin polypeptides exemplified herein, more preferably at least approximately 80% identity, most preferably at least approximately 90% identity. Such functionally active variants and fragments include, for example, those having conservative amino acid substitutions of one or more residues in the corresponding amino acid sequence. Preferably the fragment has a size of at least 10 amino acids, more preferably at least 15 amino acids, most preferably at least 20 amino acids.

[0032]By "operatively linked" is meant that a regulatory element is capable of causing expression of said nucleic acid in a cell and/or a terminator is capable of terminating expression of said nucleic acid in a cell. Preferably, said regulatory element is upstream of said nucleic acid and said terminator is downstream of said nucleic acid.

[0033]By "an effective amount" is meant an amount sufficient to result in an identifiable phenotypic trait in said plant, or a plant, plant seed or other plant part derived therefrom. Such amounts can be readily determined by an appropriately skilled person, taking into account the type of plant, the route of administration and other relevant factors. Such a person will readily be able to determine a suitable amount and method of administration. See, for example, Maniatis et al, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, the relevant disclosure of which is incorporated herein by reference.

[0034]It will also be understood that the term "comprises" (or its grammatical variants) as used in this specification is equivalent to the term "includes" and should not be taken as excluding the presence of other elements or features.

[0035]The construct of the present invention may be a vector. In a preferred embodiment of this aspect of the invention, the vector may include at least one regulatory element, such as a promoter, operatively linked to the nucleic acid. The vector may also include an operatively linked terminator.

[0036]The vector may be of any suitable type and may be viral or non-viral. The vector may be an expression vector. Such vectors include chromosomal, non-chromosomal and synthetic nucleic acid sequences, eg. derivatives of plant viruses; bacterial plasmids; derivatives of the Ti plasmid from Agrobacterium tumefaciens, derivatives of the Ri plasmid from Agrobacterium rhizogenes; phage DNA; yeast artificial chromosomes; bacterial artificial chromosomes; binary bacterial artificial chromosomes; vectors derived from combinations of plasmids and phage DNA. However, any other vector may be used as long as it is replicable, or integrative or viable in the relevant cell.

[0037]The regulatory element and terminator may be of any suitable type and may be endogenous to the target cell or may be exogenous, provided that they are functional in the target cell.

[0038]Preferably one of the regulatory elements is a promoter. A variety of promoters which may be employed in the vectors of the present invention are well known to those skilled in the art. Factors influencing the choice of promoter include the desired tissue specificity of the vector, and whether constitutive or inducible expression is desired and the nature of the cell to be transformed. Particularly suitable constitutive promoters for use in plants include the Cauliflower Mosaic Virus 35S (CaMV 35S) promoter, the maize Ubiquitin promoter, and the rice Actin promoter. In a preferred embodiment the promoter may be chosen to enable the expression of oleosin in the desired organ, tissue and stage of development.

[0039]A variety of terminators which may be employed in the vectors of the present invention are also well known to those skilled in the art. The terminator may be from the same gene as the promoter sequence or a different gene. Particularly suitable terminators for use in plants are polyadenylation signals, such as the CaMV 35S polyA and other terminators from the nopaline synthase (nos) and the octopine synthase (ocs) genes.

[0040]The vector, in addition to the regulatory element, the nucleic acid and the terminator, may include further elements necessary for expression of the nucleic acid, in different combinations, for example vector backbone, origin of replication (ori), multiple cloning sites, spacer sequences, enhancers, introns (such as the maize Ubiquitin Ubi intron), antibiotic resistance genes and other selectable marker genes (such as the neomycin phosphotransferase (npt2) gene, the hygromycin phosphotransferase (hph) gene, the phosphinothricin acetyltransferase (bar or pat) gene), and reporter genes (such as green fluorescence protein (GFP), beta-glucuronidase (GUS) gene (gusA)). The vector may also contain a ribosome binding site for translation initiation. The vector may also include appropriate sequences for facilitating correct transcription, amplifying expression, increasing mRNA stability, enhancing protein translation or facilitating accurate translation.

[0041]As an alternative to use of a selectable marker gene to provide a phenotypic trait for selection of transformed host cells, the presence of the construct or vector in transformed cells may be determined by other techniques well known in the art, such as PCR (polymerase chain reaction), Southern blot hybridisation analysis, histochemical GUS assays, northern and Western blot hybridisation analyses.

[0042]Those skilled in the art will appreciate that the various components of the construct or vector are operatively linked; so as to result in expression of said nucleic acid. Techniques for operatively linking the components of the construct or vector of the present invention are well known to those skilled in the art. Such techniques include the use of linkers, such as synthetic linkers, for example including one or more restriction enzyme sites.

[0043]The constructs and vectors of the present invention may be incorporated into a variety of plants, including monocotyledons (such as grasses from the genera Lolium, Festuca, Paspalum, Pennisetum, Panicum and other forage and turfgrasses, corn, rice, sugarcane, oat, wheat and barley) dicotyledons (such as arabidopsis, tobacco, soybean, canola, cotton, potato, chickpea, medics, white clover, red clover, subterranean clover, alfalfa, eucalyptus, poplar, hybrid aspen, and gymnosperms (pine tree)). In a preferred embodiment, the constructs and vectors are used to transform commercial crops that are fed directly to animals.

[0044]The constructs and vectors of the present invention may also be incorporated into other eukaryotic expression systems, including yeast, insect and mammalian cells. Thus, repeat oleosins, such as multimeric tandem repeat oleosins, (either homo or hetero repeats) may be generated by recombinant protein expression in eukaryotic expression systems and subsequently purified as functional recombinant oil bodies having the additional properties afforded by the presence of repeat oleosins.

[0045]The constructs and vectors of the present invention may also be incorporated into prokaryotic expression systems. Thus, repeat oleosins, such as multimeric tandem repeat oleosins, (either homo or hetero repeats) may be generated by recombinant protein expression in bacteria such as Escherichia coli and subsequently purified and recombined with for example, phospholipids and triacyl glyceride to generate functional recombinant oil bodies with the additional properties afforded by the presence of repeat oleosins.

[0046]The constructs and vectors of the present invention may be constructed by any suitable method, including: [0047]Amplification and subsequent cloning of oleosin sequences, for example using PCR with primers designed to publicly available oleosin sequences. For plant based expression clones these may include oleosins amplified from genomic DNA that may also contain introns depending on the clone. For prokaryotic and non-plant eukaryotic expression systems the source of the template for PCR preferably comes from cDNA which will not contain plant introns. [0048]Restriction digestion and ligation of oleosin clones that contain suitable inframe restriction sites at both N and C termini. Restriction sites may be added by techniques such as PCR or ligation of sticky ends. [0049]Engineering different restriction sites (that correspond to a cloning polylinker sequence) onto the ends of individual oleosin clones, then building up the multimer by a series of digestions and ligations by firstly ligating the polylinker to the 3' end of the first oleosin clone. [0050]Chemically synthesising the complete construct. [0051]A combination of the above.

[0052]Techniques for incorporating the constructs and vectors of the present invention into cells (for example by transduction, transfection or transformation) are well known to those skilled in the art. For plant cells, techniques include Agrobacterium mediated introduction, electroporation to tissues, cells and protoplasts, protoplast fusion, injection into reproductive organs, injection into immature embryos and high velocity projectile introduction to cells, tissues, calli, immature and mature embryos. The choice of technique will depend largely on the type of cell to be transformed.

[0053]Cells incorporating the constructs and vectors of the present invention may be selected, as described above, and then cultured in an appropriate medium to regenerate transformed plants, using techniques well known in the art. The culture conditions, such as temperature, pH and the like, will be apparent to the person skilled in the art. The resulting plants may be reproduced, either sexually or asexually, using methods well known in the art, to produce successive generations of transformed plants.

[0054]In a further aspect of the present invention there is provided a plant cell, plant, plant seed or other plant part, including, e.g. transformed with, a construct or vector of the present invention.

[0055]The plant cell, plant, plant seed or other plant part may be from any suitable species, including monocotyledons, dicotyledons and gymnosperms. In a preferred embodiment the plant cell, plant, plant seed or other plant part is from a commercial plant that is normally fed directly to animals.

[0056]The present invention also provides a plant, plant seed or other plant part derived from a plant cell of the present invention and including a construct or vector of the present invention. The present invention also provides a plant, plant seed or other plant part derived from a plant of the present invention and including a construct or vector of the present invention.

[0057]The present invention also provides a eukaryotic cell, such as a yeast, insect or mammalian cell, including, eg. transformed with, a construct or vector of the present invention.

[0058]The present invention also provides a prokaryotic cell, eg. a bacteria such E. Coli, including, eg. transformed with, a construct or vector of the present invention.

[0059]The present invention also provides a method of producing repeat oleosins in a plant, said method including introducing into said plant a construct or vector of the present invention. By "repeat oleosin" is meant a recombinant polypeptide including two or more oleosin repeat units.

[0060]The present invention also provides a method of producing repeat oleosins in a eukaryotic cell, said method including introducing into said eukaryotic cell a construct or vector of the present invention. The method may include the further step of partially or substantially purifying said repeat oleosin from said cell. In a preferred form the repeat oleosin may be partially or substantially purified by the generation of oil bodies. The oil bodies may be produced within the cell, e.g. plant seed.

[0061]The present invention also provides a method of producing repeat oleosins in a prokaryotic cell, said method including introducing into said prokaryotic cell a construct or vector of the present invention. The method may include the further steps of partially or substantially purifying said repeat oleosin from said cell. In a preferred form the repeat oleosin may be partially or substantially purified by the generation of oil bodies. The oil bodies may be produced artificially using recombinant oleosin repeats from other expression systems such as E. coli.

[0062]The oleosin protein repeats may be purified using affinity chromatography, such as a fused Histidine tag and Ni.sup.2+ resin purification.

[0063]The present invention also provides a partially or substantially purified and/or recombinant polypeptide including two or more oleosin repeat units.

[0064]The polypeptide may be produced by expression of a construct or vector according to the present invention.

[0065]The present invention also provides a lipid encapsulated by a polypeptide according to the present invention.

[0066]The oleosin repeat units may be of any suitable type, including functionally active fragments and variants thereof. For example, the oleosin repeat units may be selected from the group consisting of L-oleosin, H-oleosin, steroleosin and caoleosin and functionally active fragments and variants thereof. The oleosin repeats may be tandem repeats. The oleosin repeats may be multimeric tandem repeats. The oleosin repeats may be homo- or hetero-repeats.

[0067]In a preferred embodiment, the oleosin repeat unit may be from white clover or sesame seed, or may be a synthetic or recombinant version of an oleosin repeat unit from white clover or sesame seed. However, the invention is not limited thereto and the polypeptide of the present invention may include any functionally active plant oleosin sequence.

[0068]The oleosin repeat units may be linked either directly or by linking sequences. Thus, the polypeptide may further include linking sequences between two or more of the oleosin repeat units. The linking sequences may allow flexibility, induce a directional change or enable degradation between the oleosin repeat units.

[0069]In a particularly preferred embodiment of the present invention, the oleosin repeat unit includes an amino acid sequence selected from the group consisting of the sequences shown in FIGS. 69, 70, 78-83 and 107-116 hereto, and functionally active fragments and variants thereof.

[0070]In another particularly preferred embodiment of the present invention, the oleosin repeat unit is encoded by a nucleotide sequence selected from the group consisting of sequences shown in FIGS. 13, 15, 17, 19, 21, 23, 25, 27, 31, 34, 70, 72-77 and 97-106 hereto, and functionally active fragments and variants thereof.

[0071]The recombinant polypeptide of the present invention includes two or more oleosin repeats, preferably between two or three and twenty oleosin repeats, more preferably between two or three and ten oleosin repeats, most preferably between two or three and five or six oleosin repeats.

[0072]Applicants have found that that repeat oleosins, such as recombinant multimeric tandem repeat oleosins, (either homo or hetero repeats) may be expressed in the seeds of plants which would mean that the extract would contain a mixture of native oleosins along with the repeat oleosins. If a single species of oleosin multiples are required the repeat oleosins may be expressed in plants in which native oleosin expression has been suppressed, e.g., by mutagenesis, gene silencing or natural selection.

[0073]In addition, the repeat oleosins may be coexpressed with a diacylglyerol acyltransferase such as DGAT1 or DGAT2 or PDAT, in plant vegetative organs allowing the generation of emulsion complexes containing substantially only the desired species of oleosin (since oleosins are not normally expressed in the vegetative portions of plants). Thus, co-expression of DGAT1, DGAT2 or PDAT with polyoleosin in the vegetative portions of plants produces oil bodies encapsulated by the polyoleosin.

[0074]Furthermore, the repeat oleosins may be expressed and purified from bacteria, such as E. coli, since oleosins are not naturally present in E. coli. Expression of repeat oleosins in some bacteria may require modification of the nucleotide sequence to avoid recombination events occurring in rec.sup.- strains.

[0075]Applicants have found that use of a series of oleosin repeats generates a recombinant protein with exploitable properties. Linking oleosin units to give homo or hetero multimeric repeats reduces the number of N-termini available for the initiation amino peptidase degradation in the rumen and/or stomach as well as altering the physiochemical characteristics (e.g., the hydrophobic interactions) of the protein and thus broadening the range of emulsification properties. In particular, this has a number of exploitable benefits, including: [0076]Generating a simple method for producing foodstuffs such as meat and milk with health promoting lipid profiles by reducing the degree of biohydrogenation. [0077]Allowing for the delivery of fused bioactive peptides to be ingested and delivered intact to the site of absorption. [0078]Providing a rapid mechanism to alter the emulsion properties of reconstituted feeds, pharmaceuticals, beauty products etc. [0079]Allowing for the delivery of lipid soluble active compounds to be delivered and released in a controlled fashion by topical application. [0080]Allowing for the delivery of lipid soluble bioactive compounds to be ingested and delivered intact to the site of absorption.

[0081]Applicants have found that by the use of repeat oleosins, such as recombinant multimeric tandem repeat oleosins (either homo or hetero repeats) the stability of an oil body may be regulated. The incorporation of amino acid residues between the oleosin repeats may be desirable to allow sufficient flex between the repeats, to influence the curvature of the oil body, to control the direction of the repeats relative to each other, to incorporate bioactive peptides, to provide sites for directed proteolytic degradation, or to provide sites for specific enzymatic cleavage and subsequent fusion, e.g., modified self splicing intein and polymerisation cyclisation (Williams et al., 2005).

[0082]Thus, the present invention also provides a mechanism for the delivery of bioactive peptides that may be fused between the repeats or at the end of the repeats.

[0083]The present invention also provides a mechanism for allowing free rotation between the repeats or for directing the orientation of the repeats relative to each other by incorporating linking sequences between the repeats.

[0084]The size of the suspended particles contributes to the stability of the suspension and the amount of material that may be suspended and this allows the emulsification properties to be tailored for the application. By altering the number of oleosin repeats in a peptide sequence (preferably using recombinant technologies) oleosins with different emulsification properties may be generated. These may confer enhanced stabilities in terms of, for example, temperature stability, pH stability and/or altered particle size. In turn this broadens the number of compounds that may be emulsified, as well as expanding the applications of the emulsifications, for example, by extending their stability and the amount of compounds that may be emulsified.

[0085]In a further aspect the present invention provides a method of manipulating lipids in a plant, said method including introducing into said plant a construct including one or more nucleic acids encoding two or more oleosin repeat units.

[0086]Manipulation of lipids includes, but is not limited to, alteration of emulsification properties, including stability of suspension and amount of material that may be suspended, alteration of physiochemical properties, including hydrophobic interactions, and altering the degree of biohydrogenation.

[0087]In a preferred embodiment, the present invention provides a method of altering stability of an oil body in a plant, said method including modifying an oleosin in said plant to include two or more oleosin repeat units. This may in turn alter the ratio of oleosin to oil in said oil body.

Reduction of Biohydrogenation

[0088]In ruminants, biohydrogenation is the hydrogenation of non-reduced compounds (such as unsaturated fats) with hydrogen from rumen biota. Applicants have engineered oleosin to generate oil bodies containing unsaturated fats in the TAG (surrounded by a phospholipid monolayer) encapsulated by the oleosin repeats of the present invention. This may be less susceptible to the process of biohydrogenation in the rumen before it passes into the intestine for absorption. While applicants do not wish to be restricted by theory, it is thought that a chain of oleosin units would have fewer N-termini per unit of oleosin available for amino peptidase degradation (the main form of protein degradation in the rumen). In turn this would reduce the degree of oleosin degradation and therefore reduce the loss of oil body integrity and subsequently reduce the degree of biohydrogenation of the unsaturated fats in the TAG. In turn this would lead to an increase in the level of unsaturated fats reaching the site of adsorption in the intestine. In turn this would lead to a change in the fatty acid profile of foodstuffs such as milk and meat products from the animal eating such a product.

[0089]Thus, the present invention provides a method of altering biohydrogenation of a lipid, said method including encapsulating said lipid in a recombinant polypeptide including two or more oleosin repeat units.

[0090]The present invention also provides a method of protecting unsaturated lipids from biohydrogenation, said method including incorporating said unsaturated lipids into an oil body including a recombinant polypeptide including two or more oleosin repeat units.

Delivery of Fused Bioactive Peptides Orally and Topically

[0091]Applicants have engineered restriction sites between the oleosin repeats to enable insertion of a frame coding sequence (such as those encoding bioactive peptides that would normally be susceptible to degradation in the intestines). While applicants do not wish to be restricted by theory it is thought that a chain of oleosin units would have enhanced stability in the digestive acid conditions of the stomach as well as fewer N-termini per unit of oleosin available for amino peptidase degradation (the main form of protein degradation in the rumen). Thus a peptide inserted between multimeric oleosin tandem repeats is afforded a degree of protection from degradation by digestive acidic conditions and aminopeptidases. In turn this would reduce the degree of active peptide degradation in the stomach and rumen. In turn this would lead to higher levels of active peptides reaching the site of adsorption in the intestine. In turn this would lead to an increased absorption of bioactive peptides by the organism. The degree of protection may be altered by the position of the bioactive peptide in the oleosin chain, the nature of the oleosins in the chain, and/or the amino acid sequences joining the oleosins and bioactive peptides.

[0092]Thus, the present invention provides a method of delivering a bioactive peptide, to animals including humans, said method including inserting said peptide at the N- or C-terminus of a series of two or more oleosin repeat units or between two or more oleosin repeat units to produce a recombinant polypeptide and administering said recombinant polypeptide to said animal.

[0093]Preferably, the bioactive peptides are delivered orally or topically. The bioactive peptides may be delivered to the intestine. The bioactive peptides may be delivered by timed release, eg. sustained release or delayed release.

[0094]The present invention also provides a partially or substantially purified or recombinant polypeptide including two or more oleosin repeat units and further including one or more bioactive peptides.

[0095]The bioactive peptide may be inserted at the N- or C-terminus of a series of two or more oleosin repeat units or between two or more oleosin repeat units.

[0096]The recombinant polypeptide may be produced by expression of a construct or vector according to the present invention.

[0097]Thus, the present invention also provides a construct including one or more nucleic acids encoding two or more oleosin repeat units and further including one or more nucleic acids encoding bioactive peptides.

Delivery of Encapsulated Bioactive Peptides and Other Compounds Orally and Topically

[0098]Polyoleosin provides a mechanism for the development and delivery of compounds such as therapeutic and prophylactic drugs, including drugs for internal parasites in humans and animals and bioactive peptides; and organisms such as health promoting bacteria (e.g., lactobacillus) by encapsulation of the compound or organism within the oil body. In particular, it provides a mechanism for delivering bioactive peptides through the rumen and into the digestive system, substantially without loss of bioactivity. This issue currently represents a major hurdle for the development of bioactives for internal parasites in rumens. Polyoleosins thus facilitate development of bioactive drug development and delivery.

[0099]In addition, polyoleosin has a similar application in the delivery of encapsulated bioactives in cosmetics, eg. creams and may be applied epidermally, for example to wounds or skin problems. Polyolesin may also have applications for controlled release in dermal applications.

[0100]Thus, the present invention also provides a method of delivering compounds and/or organisms to animals including humans, said method including encapsulation said compound or organism in an oil body including two or more oleosin repeat units and administering said oil body to said animal.

[0101]Preferably the compound is a therapeutic or prophylactic drug or a bioactive peptide or protein.

[0102]Preferably the organism is a bacterium, more preferably a health promoting bacterium such as lactobacillus.

[0103]Preferably the compound or organism is delivered orally or topically. The compound or organism may be delivered to the intestine. The compound or organism may be delivered by timed release eg. sustained release or delayed release.

Emulsification and Encapsulation of Bioactives

[0104]Repeat oleosins, such as recombinant multimeric tandem repeat oleosins (either homo or hetero repeats), may be used to tailor emulsion complexes and to encapsulate bioactive compounds that may exist in the emulsion. By the use of repeat oleosins, the stability of an oil body may be tailored by oleosin. The size of the suspended particles contributes both to the stability of the suspension and the amount of material that may be suspended. By altering the number of oleosin repeats in a peptide sequence (preferably using recombinant technologies) oleosins with different emulsification properties are generated. These confer enhanced stabilities in terms of, for example, temperature and pH stability and altered particle size. In turn this broadens the number of compounds that may be emulsified as well as expanding the applications of the emulsifications.

[0105]Polyoleosin allows the manufacturer to tailor the emulsification properties by altering the number of oleosin repeats. The majority of processed foods utilise emulsifiers of some form or another. In addition, polyoleosins may be utilised in the cosmetics industry. The oil based encapsulation mechanism provides an ideal delivery mechanism for any compound, notably bioactives for dermal application.

[0106]Accordingly, in a further aspect the present invention provides a method of altering the emulsification properties of an oleosin, said method including recombinantly producing the oleosin with two or more oleosin repeat units.

[0107]Altering the emulsification properties of the oleosin may include altering temperature and/or pH stability and/or size of oil bodies including the oleosin.

[0108]The present invention also provides a recombinant oleosin with altered emulsification properties, said oleosin including two or more oleosin repeat units.

[0109]The recombinant polypeptide may be produced by expression of a construct or vector according to the present invention.

[0110]Thus, in the polypeptides of the present invention tandem oleosins may be fused directly or by small linking (eg. hinge) sequences. The polypeptides may contain fused bioactive peptides either at the terminal ends of the repeats or located between the repeats.

[0111]Such polyoleosins may be used to deliver encapsulated products/compounds/proteins that do not have to be fused to the oleosin peptides but rather are generated during the process of creating oil bodies or AOBs.

[0112]Polyoleosins may also be used to deliver bioactive peptides either encapsulated within oil bodies, AOBs or fused to the ends of oleosin repeats or fused between the repeats.

[0113]Polyoleosins used for emulsification or delivery or protection of compounds may be tailored by changing the number of oleosin tandem repeats rather than simply being the fusion of a peptide of insert fused between two oleosin repeats.

[0114]The present invention will now be more fully described with reference to the accompanying Examples and drawings. It should be understood, however, that the description following is illustrative only and should not be taken in any way as a restriction on the generality of the invention described above.

IN THE FIGURES

[0115]FIG. 1. Kyte and Doolittle hydrophobic plot (window=17) of a typical oleosin sequence.

[0116]FIG. 2. Oil body showing topology of oleosin single peptide chains.

[0117]FIG. 3. Oil body showing topology of dimeric oleosin repeat peptide chains joined by unique peptide linkers.

[0118]FIG. 4. Oil body showing topology of trimeric oleosin repeat peptide chains joined by unique peptide linkers.

[0119]FIG. 5. Oil body showing topology of tetrameric oleosin repeat peptide chains joined by unique peptide linkers.

[0120]FIG. 6. Oil body showing topology of pentameric oleosin repeat peptide chains joined by unique peptide linkers.

[0121]FIG. 7. Typical Kyte and Doolittle hydrophobicity plot (window=17) of homo or hetero pentameric oleosin tandem repeat containing unique inter oleosin peptide liners.

[0122]FIG. 8. pBLUESCRIPT II SK MCS sequence and translated amino acid sequence. With the exception of EcoRV all other restriction sites are not present in either the white clover oleosin clone or the Gateway PCR entry vector pENTR/D .cndot. and XXX=codon not part of a restriction site.

[0123]FIG. 9. Standard layout of primers and PCR products to generate white clover polyoleosin constructs.

[0124]FIG. 10. Map of pENTR/D-TOPO.

[0125]FIG. 11. Map of pCR2.1-TOPO.

[0126]FIG. 12. Map of pOLE01-MC.

[0127]FIG. 13. Sequence of the oleosin coding region in pOLE01-MC (Seq ID No. 29). CACC=GATEWAY.TM. adapter, XXXX=oleosin sequence, XXXXXX=restriction enzyme site--included in primer, TGA=stop codon.

[0128]FIG. 14. Map of pOLE02-MC.

[0129]FIG. 15. Sequence of the oleosin coding region in pOLE02-MC (Seq ID No. 30). XXXX=oleosin sequence, XXXXXX=restriction enzyme site--included in primer, XXXXXX=codons for extra amino acids--included in primer.

[0130]FIG. 16. Map of pOLE03-MC.

[0131]FIG. 17. Sequence of the oleosin coding region in pOLE03-MC (Seq ID No. 31). XXXX=oleosin sequence, XXXXXX=restriction enzyme site--included in primer, XXXXXX=codons for extra amino acids--included in primer.

[0132]FIG. 18. Map of pOLE04-MC.

[0133]FIG. 19. Sequence of the oleosin coding region in pOLE04-MC (Seq ID No. 32). XXXX=oleosin sequence, XXXXXX=restriction enzyme site--included in primer, XXXXXX=codons for extra amino acids--included in primer.

[0134]FIG. 20. Map of pOLE05-MC.

[0135]FIG. 21. Sequence of the oleosin coding region in pOLE05-MC (Seq ID No. 33). XXXX=oleosin sequence, XXXXXX=restriction enzyme site--included in primer, XXXXXX=codons for extra amino acids--included in primer.

[0136]FIG. 22. Map of pOLE06-MC.

[0137]FIG. 23. Sequence of the oleosin coding region in pOLE06-MC (Seq ID No. 34). XXXX=GATEWAY.TM. adapter sequence, XXXX=oleosin sequence, XXXXXX=base pairs encoding for additional amino acids--included in primer, XXXX=polylinker sequence,

##STR00001##

[0138]FIG. 24. Map of pOLE07-MC.

[0139]FIG. 25. Sequence of the oleosin coding region in pOLE07-MC (Seq ID No. 35). XXXX=GATEWAY.TM. adapter sequence, XXXX=oleosin sequence, XXXXXX=base pairs encoding for additional amino acids--included in primer, XXXX=polylinker sequence,

##STR00002##

[0140]FIG. 26. Map of pOLE08-MC.

[0141]FIG. 27. Sequence of the oleosin coding region in pOLE08-MC (Seq ID No. 36). XXXX=GATEWAY.TM. adapter sequence, XXXX=oleosin sequence, XXXXXX=base pairs encoding for additional amino acids--included in primer, XXXX=polylinker sequence,

##STR00003##

[0142]FIG. 28. Agarose gel of HindIII/ClaI digested pOLE04-MC and pOLE08-MC. Dotted boxes outline the regions excised for extraction from gel.

[0143]FIG. 29. Map of pOLE09-MC.

[0144]FIG. 30. Agarose gel results from checking pOLE09-MC.

[0145]Expected Sizes: [0146]Clone 7 [0147]NcoI/XhoI--2.6 kb and 1.3 kb [0148]NcoI/SpeI/XhoI--2.6 kb, 1.3 kb & 57 bp [0149]NotI/XhoI--2.6 kb, 697 bp, & 643 bp [0150]XhoI--3.9 kb [0151]Clone 9 [0152]NcoI/XhoI--two bands at .about.2.6 kb clones C9.1-C9.3 correct [0153]NcoI/SpeI/XhoI--2.6 kb & two bands at .about.1.3 kb clones C9.1-C9.3 correct [0154]NotI/XhoI--2.6 kb, 1.9 kb & 643 bp clones C9.1-C9.3 correct [0155]XhoI--5.2 kb clones C9.1-C9.3 correct

[0156]Clones 9.1-9.3 all showed the correct/expected sizes for pOLE09-MC.

[0157]The region in the pOLE09-MC cassette containing the newly inserted oleosin was then sequenced.

[0158]FIG. 31. Sequence of pOLE09-MC, confirming the addition of the oleosin from pOLE04-MC into pOLE08-MC. Sequence was obtained by sequencing across the last oleosin in pOLE09-MC into the original pOLE08-MC vector. All mismatches were checked back to the original electropherogram to confirm errors were due to software misreads.

[0159]FIG. 32. Map of pOLE10-MC.

[0160]FIG. 33. Agarose gel analysis of a restriction enzyme digested pOLE10-MC clone, compared to pOLE09-MC.

[0161]Expected Sizes:

TABLE-US-00001 Clone 9 XhoI/PstI -4.5 kb and 650 bp correct PstI -5.1 kb correct SalI/PstI -4.5 kb and 650 bp correct

[0162]Expected Sizes:

TABLE-US-00002 Clone 10 XhoI/PstI -4.5 kb and 1.2 kb correct PstI -5.7 kb correct SalI/PstI -5.1 kb and 650 bp correct

[0163]Both pOLE09-MC and pOLE10-MC clones were found to be correct when analysed by restriction digests.

[0164]The region in the pOLE10-MC cassette containing the newly inserted oleosin was then sequenced using the M13-Reverese primer (five clones sequenced and found to match the predicted sequence.

[0165]FIG. 34. Sequence of pOLE10-MC, confirming the addition of the oleosin from pOLE05-MC, into pOLE09-MC. Sequence was obtained via sequencing into the fifth pOLE10-MC and back across into pOLE09-MC. FIG. 35. Map of pRSh1.

[0166]FIG. 36. Map of pRS12.

[0167]FIG. 37. EcoRI digest of C6 and C7 clones in pRSH1.

[0168]Expected Sizes:

TABLE-US-00003 Clone 6-pRSH1 10,349 bp, 3084 bp, 725 bp and 566 bp clones 1, 3, &4 correct Clone 7-pRSH1 10,349 bp, 3084 bp, 1352 bp and clones 1, 2, 566 bp &3 correct pRSH1 11,525 bp, 3084 bp, 566 bp and 463 bp.

[0169]FIG. 38. EcoRI digest of C8 clones in pRSH1.

[0170]Expected Sizes:

TABLE-US-00004 Clone 8-pRSH1 10,349 bp, 3084 bp, 1973 bp and 566 bp clones 2-8 correct pRSH1 11,525 bp, 3084 bp, 566 bp and 463 bp.

[0171]FIG. 39. EcoRI digest of C9 and C10 clones in pRSH1.

[0172]Expected Sizes:

TABLE-US-00005 Clone 9-pRSH1 10,970 bp, 3084 bp, 1973 bp and clones 1, 2, & 566 bp 4 correct Clone 10-pRSH1 11,594 bp, 3084 bp, 1973 bp and clones 1, 2, & 566 bp 4 correct.

[0173]FIG. 40. BamHI digest of C9 and C10 clones in pRSH1.

[0174]Expected Sizes:

TABLE-US-00006 Clone 9-pRSH1 10826 bp, 4400 bp and 1367 bp clone correct Clone 10-pRSH1 10826 bp, 4400 bp and 1991 bp clone correct pRSH1 10826 bp, 3279 bp, 830 bp and 703 bp.

[0175]FIG. 41. EcoRI digest of DGAT1 clones in pRSH1.

[0176]Expected Sizes:

TABLE-US-00007 DGAT1-pRSH1 10700 bp, 3084 bp, clones 1-3 correct 1232 bp and 566 bp pRSH1 11525 bp, 3084 bp, FIG. 42. EcoRV digest of 566 bp and 463 bp. C6 clones in pRS12.

[0177]Expected Sizes:

TABLE-US-00008 C6-pRS12 9131 bp, 7424 bp and 3762 bp clones 2, 3, 5, &8 correct pRS12 13810 bp and 7424 bp.

[0178]FIG. 43. Restriction digest of DGAT1 and C7 clones in pRS12.

[0179]Expected Sizes:

TABLE-US-00009 DGAT1-pRS12 SpeI 14437 bp, 3833 bp clones 1 &2 and 2908 bp correct C7-pRS12 SpeI 14437 bp, 2908 bp, 2724 bp clones 1 &2 and 878 bp correct pRS12 SpeI 14437 bp, 3889 bp and 2908 bp DGAT1-pRS12 BamHI 17039 bp clones 1 &2 and 4139 bp correct C7-pRS12 BamHI 16683 bp, 4139 bp clones 1 &2 and 125 bp correct pRS12 BamHI 15562 bp, 4139 bp, 830 bp and 703 bp.

[0180]FIG. 44. Restriction digest of C8, C9 and C10 clones in pRS12.

[0181]Expected Sizes:

TABLE-US-00010 C8-pRS12 SpeI 14437 bp, 2908 bp, 2724 bp clones 1 &2 and 1499 bp correct C9-pRS12 SpeI 14437 bp, 2908 bp, 2724 bp clones 2 &3 and 2120 bp correct C10-pRS12 SpeI 14437 bp, 2908 bp, 2744 bp clones 1-3 and 2724 bp correct pRS12 SpeI 14437 bp, 3889 bp and 2908 bp C8-pRS12 BamHI 16683 bp, 4139 bp clones 1 &2 and 746 bp correct C9-pRS12 BamHI 16683 bp, 4139 bp clones 2 &3 and 1367 bp correct C10-pRS12 BamHI 16683 bp, 4139 bp clone 1 . . . and 1991 bp correct pRS12 BamHI 15562 bp, 4139 bp, 830 bp and 703 bp.

[0182]FIG. 45. Restriction digest of C8, C9 and C10 clones in pRS12.

[0183]Expected Sizes:

TABLE-US-00011 C10-pRS12 BamHI 16683 bp, 4139 bp and 1991 bp clones . . . 2 & 3 correct C8-pRS12 EcoRV 10382 bp, 7424 bp and 3762 bp clones 1 & 2 correct C9-pRS12 EcoRV 10382 bp, 7424 bp and 4383 bp clones 2 & 3 correct C10-pRS12 EcoRV 10382 bp, 7424 bp and 5007 bp clones 1-3 correct pRS12 SpeI 14437 bp, 3889 bp and 2908 bp pRS12 BamHI 15562 bp, 4139 bp, 830 bp and 703 bp pRS12 EcoRV 13810 bp and 7424 bp.

[0184]FIG. 46. A representative diagram of the pRSh1 binary vector containing oleosin multimers.

[0185]FIG. 47. A representative diagram of the pRS12 binary vector containing oleosin multimers.

[0186]FIG. 48. Plasmid map for the expression vector p17NON (N terminal oleosin, in pDEST17).

[0187]FIG. 49. Plasmid maps for the expression vectors p42CON (N terminal oleosin in pET DEST42).

[0188]FIG. 50. Characterisation of p17NON by PCR analysis.

[0189]Expected Sizes: NT -505 bp

[0190]All plasmids appear to contain an insert of the expected size

[0191]This amplification confirms the presence of the N terminal oleosin gene in the pDEST17 plasmid.fwdarw.p17NON

[0192]FIG. 51. Characterisation of p42CON by PCR analysis.

[0193]Expected Sizes: NT -561 bp [0194]NT#1 appears to contain a slightly larger insert.

[0195]All others appear to contain an insert of the expected size

[0196]This amplification confirms the presence of the N-terminal oleosin gene in the pET DEST42 plasmid.fwdarw.p42CON

[0197]FIG. 52. Expression analysis by SDS PAGE of 6HON. N=Non-induced [0198]I=Induced <=putative expressed 6HON expected size 6HON=14.7 kD.

[0199]FIG. 53. Inclusion body analysis by SDS PAGE of the 6HONpeptide. N=Non induced, I=Induced, <=putative expressed 6HON, expected size 6HON=14.7 kD

*=putative expressed 6HOC expected size 6HOC=12.8 kD

[0200]FIG. 54. Trial scale Nickel column purification analysis by SDS PAGE of 6HON. <=putative expressed 6HON expected size 6HON=14.7 kD.

[0201]Samples loaded as equivalent volumes.

[0202]FIG. 55. Large scale Nickel purification analysis by SDS PAGE of 6HON. Expected size of 6HON=14.7 kD.

[0203]FIG. 56. Concentration of 6HON. Volume of each eluted fraction was approximately 1 mL.

[0204]FIG. 57. SDS-PAGE/immunoblot screened against anti oleosin N terminal antibody. Run on 18% SDS PAGE gel, 90 min 150V. 1.degree. and 2.degree. antibody diluted in 20 mL PBS. 1.degree. antibody=1:2000 (10 .mu.L). 2.degree. antibody=1:5000 (4 .mu.L) anti rabbit Ig, Horseradish Peroxidase linked whole antibody from donkey.

[0205]Lanes 4, 5, and 6 contained 1.8, 6.9, and 4.7 ng purified 6HON, respectively. Antibody appears to bind to 17OF (Lane 2), 17OC (Lane 3) and a number of peptides present in the extract from clover seed. Reason for binding to 17OC unclear, but may be due to similarities in 6.times.His tag and neighbouring regions.

[0206]FIG. 58. Coomassie and subsequent immunoblot analysis of oil bodies extracted from clover seed. Arrow indicates expected size of clover seed oleosin (20 kDa).

[0207]L=Ladder; A & B=duplicate oil body extracts from clover seed.

[0208]FIG. 59. PCR analysis of Agrobacterium colonies transformed with oleosin clone plasmids. [0209]Lane A=AgR6; B=AgR 7; C=AgR 8; [0210]D=AgR9; E & F=AgR10; G, H, I=AgR 7; [0211]J, K, L=AgR 8; M, N, O=AgR 9; P=untransformed LBA4404; Q and R=AgR 7 plasmid DNA; S=1 Kb plus ladder

[0212]FIG. 60. Effect of Basta on regeneration from hypocotyl (top) and cotyledon explants (bottom).

[0213]FIG. 61. Growth of Basta resistant and sensitive shoots from DGAT co cultivated explants on 5 mg/L Basta.

[0214]FIG. 62. PCR for the bar gene on putative transgenic shoots. [0215]Lanes A and N 1 Kb plus ladder; lanes B and C DNA from AgR 6 shoots; lanes D and E DNA from AgR 7 shoots; lanes F and G DNA from AgR 8 shoots; lanes H and I DNA from AgR 9 shoots; lanes J and K DNA from AgR 10 shoots; lane L AgR 7 plasmid DNA; lane M blank

[0216]FIG. 63. PCR for the Bar and oleosin gene.

[0217]Top panel .dbd.PCR for bar gene, Bottom panel .dbd.PCR with the same DNA using oleosin clone specific primers

TABLE-US-00012 Lanes A = 1kb plus ladder; B F = pRSH1 C6 plants; G = pRSH1 C6 plasmid; H = blank; I L = pRSH1 C7 plants; M = pRSH1 C7 plasmid; N = blank; O R = pRSH1 C8 plants; S = pRSH1 C6 plasmid; T = 1kb plus ladder

[0218]FIG. 64. RT PCR for oleosin from pRSH1 C6 transgenic shoots. [0219]Lanes A and N=1 Kb plus ladder; [0220]B F=reverse transcriptase treated RNA from pRSH1 C6 plants; [0221]G K RNASE treated RNA from pRSH1 C6 plants; [0222]L=pRSH1 C6 plasmid DNA; [0223]M blank

[0224]FIG. 65. Northern blot analysis of 5 .mu.g total RNA from Lotus japonicus hairy roots transformed with 1, 2, 3, 4 or 5 oleosin repeats.

[0225]Probed with 25 ng random primed 5 .mu.Ci 32P labelled oleosin cDNA.

[0226]Positive controls: +=4 pg; +=20 pg (arrows in ladder lane); oleosin gene (PCR product).

[0227]Line in single oleosin lanes indicates main transcript size detected (approximately 1.4 Kb);

[0228]Line in tandem oleosin construct lanes indicates main transcript size detected (approximately 2 Kb);

[0229]Line in trimeric oleosin construct lanes indicates main transcript size detected (approximately 2.7 Kb);

[0230]Line in tetrameric oleosin construct lanes indicates main transcript size detected (approximately 3.4 Kb);

[0231]Line in pentameric construct lanes indicates main transcript size detected (approximately 4 Kb);

[0232]Small black arrows indicate oleosin hybridising transcripts of aberrant size.

[0233]FIG. 66. Schematic diagram of the synthetic sesame seed polyoleosin construct. The sequence was generated using optimised codons selected for expression and elevated GC content, randomised between the repeats with elevated mRNA stability, cryptic splice sites removed, UBQ10 intron, Kozak, tetranucleotide stop codon and restriction sites added.

[0234]FIG. 67. Arabidopsis thaliana UBQ10 intron modifications.

A. Modified Arabidopsis thaliana UBQ10 intron (3' splice site modified to be PstI as per Rose and Beliakoff, 2000) (Seq ID No. 44).B. Comparison of the modified UBQ10 intron (Seq ID No. 44) with the original sequence from Norris et al., (1993) (Seq ID No. 45). Consensus=Seq ID No. 46.

[0235]FIG. 68. NetGene2 graphical output prediction of splicing of the synthetic sesame seed polyoleosin construct. The GC content had been elevated, cryptic splice sites had been manually removed, and the Arabidopsis thaliana UBQ10 intron had been added.

[0236]FIG. 69. Alignment of the translated sequences of 6 tandem repeats of the original sesame seed oleosin (without linkers) (Seq ID No. 47) with the 6 tandem repeats containing random assignment of the appropriate degenerate codons, GC optimised and modified linkers (with the intron removed) (Seq ID No. 48). Consensus=Seq ID No. 49.

[0237]The alignment shows the oleosin peptide sequences of each repeat are identical, also there is no change between the randomised codons sequences with and without intron.

[0238]FIG. 70. Nucleic acid (Seq ID No. 50) and amino acid (Seq ID No. 51) Sequence and feature map of the synthetic sesame seed hexameric polyoleosin with randomised optimal degenerate codons, enriched GC content, enhanced mRNA stability, engineered restriction sites (also optimised for codon usage) and modified UBQ10 intron.

Key: attL sites (bold); engineered restriction sites and linkers (italics); oleosin repeats (grey box, white letters); double stop codon to ensure no read through due to amber codon (bold, underline); tetra-nucleotide stop codon (black box, white letter); UBQ10 intron (grey box, black letters); -20 to -11 from original cDNA (underline); -10 to -1 modified Joshi et al (1997) consensus sequence (bold, italics, underline).

[0239]FIG. 71. Vector map of the synthetic sesame seed polyoleosin construct in PCR Script.

[0240]FIG. 72. Nucleotide sequence of clone synthesised by GENEART AG containing 6 tandem Sesame seed oleosin repeats with randomised degerate codons (Seq ID No. 52).

[0241]FIG. 73. Feature map of the nucleotide sequence of the identical triple oleosin repeats synthesised by GENEART AG (Seq ID No. 53).

[0242]FIG. 74. Feature map of nucleotide sequence of pET29+Ole6-6.times.His (Seq ID No. 54).

[0243]FIG. 75. Feature map of nucleotide sequence of pET29+Ole2-6.times.His (Seq ID No. 55).

[0244]FIG. 76. Feature map of nucleotide sequence of pET29+Ole4-6.times.His (Seq ID No. 56).

[0245]FIG. 77. Feature map of nucleotide sequence of pET29+Ole5-6.times.His (Seq ID No. 57).

[0246]FIG. 78. Peptide sequence of: pET29+Ole6-6.times.His (Seq ID No. 58).

[0247]FIG. 79. Peptide sequence of: pET29+Ole2-6.times.His (Seq ID No. 59).

[0248]FIG. 80. Peptide sequence of: pET29+Ole4-6.times.His (Seq ID No. 60).

[0249]FIG. 81. Peptide sequence of: pET29+Ole5-6.times.His (Seq ID No. 61).

[0250]FIG. 82. Peptide sequence of: pUCOle3+(Seq ID No. 62).

[0251]FIG. 83. Peptide sequence of: p29Ole (Seq ID No. 63).

[0252]FIG. 84. Whole gel elution results from prokaryotic expression and purification of sesame seed oleosin.

A. Preliminary analysis of 1.times.-6.times. AOBs by SDS-PAGE separation.

[0253]Small arrows indicate expected sizes of 4.times., 5.times. and 6.times. oleosin (rectangular boxes). Large arrows indicate bands of putative polyoleosin protein corresponding to 1.times., 2, and 3.times. oleosins (oval boxes). Expected molecular weights are shown in brackets.

B. Coomassie stained SDS-PAGE gel after whole gel elution (39C_sesame_oleosin_AOBs.doc).

[0254]L.sub.K=BioRad Kaleidoscope Standards (cat# 161-0324) Pre=Coomassie stained slice of acrylamide gel prior to elution =expected size of oleosin.

[0255]FIG. 85. SDS-PAGE analysis of fractions from Ni-affinity purification of prokaryotically expressed denatured sesame seed oleosin (48C_sesame_oleosin_His_pur.doc). [0256]PI=Post Induction SPL=Supernatant, Post Lysis [0257]L=Lysate FT=Flow Through [0258]L.sub.S=BioRad Prestained SDS-PAGE Standards, Low Range (cat# 161-0305) [0259]#.sub.A & #.sub.B=Fraction number from either column A or B. [0260]=expected size of oleosin.

[0261]FIG. 86. Analysis of rabbit anti-sesame seed oleosin antiserum by immunoblot and silver staining. Analysis of antibody titre and specificity. [0262]LK=BioRad Kaleidoscope Standards (cat# 161 0324) [0263]11=3 ng of 1 A 21=13 ng 1 A 31=27 ng 1 A 41=132 ng 1 A 51=663 ng 1 A [0264]S1 & S2=sesame seed extract C=clover seed extract [0265]12=3 ng of 1B 22=14 ng 1B 32=29 ng 1B 42=143 ng 1B [0266]I=crude post-induction sample LP=BioRad Precision Plus Standard (cat# 161 0363). [0267].quadrature.=expected size of oleosin. Overflow of the standards can be seen in lanes 11 and I.

[0268]The rabbit raised antibodies show a high affinity for the affinity purified recombinant oleosin, detecting down to at least 3 ng. The antibodies also show high specificity, with no cross-reactivity against soluble seed proteins and low cross-reactivity to bacterial proteins (lane 1).

[0269]FIG. 87. Visualisation of emulsification layer containing artificial oil bodies (AOBs) after first (top) and second (bottom) rounds of sonication.

[0270]FIG. 88. SDS-PAGE/immunoblot analysis of AOB 1.times., 2.times., 3.times., 4.times. and 6.times. oleosin.

[0271]For analysis of the 6.times. polyoleosin two samples were loaded per lane. .sub.N=non-induced negative control.

[0272]FIG. 89. Analysis of AOBs containing 1.times.-6.times. Sesame seed polyoleosin proteins by SDS/urea-Gradient PAGE/SafeStain.

[0273]FIG. 90. SDS, urea-PAGE/immunoblot of AOB Analysis of 1.times.-6.times. AOBs by SDS/urea-PAGE/SafeStain.

[0274]Small arrow indicates expected position of 6.times. oleosin (rectangular box). Large arrows indicate bands of putative polyoleosin protein corresponding to 1.times., 2, 3.times., 4.times., and 5.times. oleosins (oval boxes). Expected molecular weights are shown in brackets.

[0275]FIG. 91. Microscopic analysis of AOB containing a different number of oleosin repeats. Size of AOBs when prepared with polyoleosins containing increasing numbers of repeating oleosin units.

[0276]FIG. 92. Effect of polyoleosin on the stability over time of AOB containing a different number of oleosin repeats after 7 days at 4.degree. C. AOBs were prepared with different polyoleosins containing increasing numbers of repeating oleosin units. Vector control AOBs were prepared using inclusion bodies from E. coli containing a vector control.

[0277]FIG. 93. Microscopic analysis of size of AOB containing a different number of oleosin repeats after heat treatment at 90.degree. C. for 15 min.

[0278]FIG. 94. Heat stability of emulsification layers (containing AOB) in relation to the number of repeat oleosin units.

[0279]FIG. 95. Microscopic analysis of AOB containing a different number of oleosin repeats after incubation in different pH buffers.

[0280]FIG. 96. SDS-PAGE/immunoblot (A) and Coomassie (B) analysis of prokaryotically produced recombinant polyoleosin purified by Artificial Oil Body or Ni.sup.2+ affinity column.

[0281]FIG. 97. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh1-PSP1 (CaMV35S driving 1 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 64).

[0282]FIG. 98. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh1-PSP3 (CaMV35S driving 3 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 65).

[0283]FIG. 99. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh1-PSP4 (CaMV35S driving 4 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 66).

[0284]FIG. 100. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh1-PSP6 (CaMV35S driving 6 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 67).

[0285]FIG. 101. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh3-PSP1 (Arabidopsis oleosin seed promoter driving 1 oleosin repeat with the UBQ10 intron in the first repeat) (Seq ID No. 68).

[0286]FIG. 102. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh3-PSP3 (Arabidopsis oleosin seed promoter driving 3 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 69).

[0287]FIG. 103. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh3-PSP4 (Arabidopsis oleosin seed promoter driving 4 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 70).

[0288]FIG. 104. Feature map of nucleotide sequence of attB flanking regions, single oleosin clone and UBQ10 in pRSh3-PSP6 (Arabidopsis oleosin seed promoter driving 6 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 71).

[0289]FIG. 105. Feature map of nucleotide sequence of attB flanking regions, identical oleosin clones in pRSh1-Ole3+ (CaMV35s promoter driving 3 identical oleosin tandem repeats; no intron) (Seq ID No. 72).

[0290]FIG. 106. Feature map of nucleotide sequence of attB flanking regions, identical oleosin clones in pRSh1-Ole3+ (Arabidopsis oleosin seed promoter driving 3 identical oleosin tandem repeats; no intron) (Seq ID No. 73).

[0291]FIG. 107. Peptide sequence of: pRSh1-PSP1 (CaMV35S driving 1 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 74).

[0292]FIG. 108. Peptide sequence of: pRSh1-PSP3 (CaMV35S driving 3 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 75).

[0293]FIG. 109. Peptide sequence of: pRSh1-PSP4 (CaMV35S driving 4 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 76).

[0294]FIG. 110. Peptide sequence of: pRSh1-PSP6 (CaMV35S driving 6 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 77).

[0295]FIG. 111. Peptide sequence of: pRSh3-PSP1 (Arabidopsis oleosin seed promoter driving 1 oleosin repeat with the UBQ10 intron in the first repeat) (Seq ID No. 78).

[0296]FIG. 112. Peptide sequence of: pRSh3-PSP3 (Arabidopsis oleosin seed promoter driving 3 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 79).

[0297]FIG. 113. Peptide sequence of: pRSh3-PSP4 (Arabidopsis oleosin seed promoter driving 4 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 80).

[0298]FIG. 114. Peptide sequence of: pRSh3-PSP6 (Arabidopsis oleosin seed promoter driving 6 oleosin tandem repeats with the UBQ10 intron in the first repeat) (Seq ID No. 81).

[0299]FIG. 115. Peptide sequence of: pRSh1-Ole3+ (CaMV35s promoter driving 3 identical oleosin tandem repeats; no intron) (Seq ID No. 82).

[0300]FIG. 116. Peptide sequence of: pRSh3-Ole3+ (Arabidopsis oleosin seed promoter driving 3 identical oleosin tandem repeats; no intron) (Seq ID No. 83).

[0301]FIG. 117. SDS-PAGE/immunoblot showing production of Sesame seed polyoleosin in Arabidopsis thaliana seeds. Analysis of oil bodies from transgenic Arabidopsis thaliana seeds over expressing varying tandem repeats of the sesame seed oleosin.

[0302]FIG. 118. SDS-PAGE/Coomassie showing crude protein extracts from Arabidopsis thaliana wild type seeds and transgenic seeds expressing Sesame seed polyoleosin.

[0303]FIG. 119. Picture of relative recombinant protein levels in Arabidopsis oil bodies and effects of different Sesame seed polyoleosin lengths on emulsification thicknesses after heating. SDS-PAGE/immunoblot analysis and emulsification stability analysis of oil bodies from transgenic Arabidopsis thaliana over expressing varying tandem repeats of the sesame seed oleosin and the increase in heat stability of the emulsification layers extracted from these transformants. The reduction in oleosin repeat numbers correlates with a decrease in the emulsification layer remaining after 24 hr at 90.degree. C., where the thickest emulsification can be seen from plants expressing the hexameric polyoleosin construct.

[0304]FIG. 120. Picture of heating effect on emulsification thicknesses of transgenic Arabidopsis oil bodies expressing different polyoleosins. Heat stability analysis of the emulsification layers from transformants expressing 1, 3 or 6 oleosin repeats. The reduction in oleosin repeat numbers correlates with a decrease in the emulsification layer remaining after 24 hr at 90.degree. C., where the thickest emulsification can be seen from plants expressing the hexameric polyoleosin construct. At 0 hrs through to 24 hrs at 90.degree. C. the higher the number of oleosin repeats correlates with a thicker emulsification layer. After 58 hrs at 90.degree. C. the oil bodies from the wild type arabidopsis has been reduced to a very thin layer with a small ring of emulsion deposited on the tube above the remaining aqueous phase. In comparison, the ring of emulsion remaining in the transformant samples is much greater.

EXAMPLES

Example 1

White Clover Polyoleosin Construction

[0305]We have generated a dimeric, trimeric, tetrameric and a pentameric homo white clover oleosin tandem repeat construct and placed these into plant binary vectors for plant transformation. The following is a description of the methods used to generate the constructs. It should be noted that the oleosin sequence used is for example only. Any oleosin sequence or combinations of oleosins, steroleosins and caoleosins and oleosin linking sequences could be used.

Overview of Experimental Approach to Generation of White Clover Oleosin Repeats

[0306]Five oleosin clones (Pole01-MC to pOLE05-MC), containing suitable restriction sites, were prepared for the subsequent generation of constructs containing oleosin repeats. In this description clones pOLE01-MC to pOLE05-MC were used to prepare monomer, dimer, trimer, tetramer and pentamer oleosin repeat constructs, pOLE06-MC to pOLE10-MC respectively. The pBLUESCRIPT polylinker (FIG. 8) was used in the preparation of pOLE01-MC to provide the multiple restriction sites required to build the oleosin repeat constructs.

Standard Method of Generating Restriction Enzyme/White Clover Oleosin Cassette

[0307]PCR products were produced using a proof-reading polymerase to amplify the existing oleosin open reading frame (609 bases) of an oleosin clone containing no SacI, XbaI, SpeI, BamHI, SmaI, PstI, EcoRI, HindIII Bsp1061, SalI or XhoI sites. For each cassette unique primers were designed to amplify the oleosin sequence and add specific flanking restriction sites (FIG. 9). Additional base pairs coding for specific amino acids were also included between the restriction site and oleosin priming sequence. In the polyoleosin peptide these amino acids could be expected to act as spacer arms enabling the individual oleosins to be separated from each other, reducing the chances of any misfolding occurring.

[0308]The oleosin PCR product to generate pOLE01-MC was then TOPO cloned into the pENTR/D-TOPO vector with the primary purpose of maintaining the flanked oleosin sequence. The oleosin PCR product to generate pOLE02, 03, 04, 05-MC was then TOPO cloned into the pCR2.1-TOPO vector with the primary purpose of maintaining the flanked oleosin sequence. Maps of the vectors used for cloning, pENTR/D-TOPO and pCR2.1-TOPO are shown in FIGS. 10 and 11, respectively.

[0309]The new construct was transformed into competent E. coli cells and plated out for single colonies. Individual colonies were cultured and the purified plasmid from these cultures was analysed by digestion with a range of suitable restriction enzymes. If no suitable colonies were identified then this process was repeated. Those colonies/plasmid preps that produced predicted patterns by restriction enzyme digestion were then sequenced across the cassette containing the oleosin insert and the resulting data compared against the predicted sequence for the construct/plasmid.

[0310]The construction of constructs pOLE01-MC to pOLE05-MC is summarised below, based on the method outlined above. Each cassette was fully sequenced after construction, with all sequences being confirmed as correct.

[0311]We have generated polyclonal antibodies to a number of white clover oleosin fragments, the generation and characterisation of these antisera is summarised below.

pOLE01-MC

##STR00004##

[0312]In the forward primer XXXX represents an oleosin specific primer that has a 5' end beginning with the first ATG site in the open reading frame.

[0313]In the reverse primer XXXX represents an oleosin specific primer that has a 5' end complementary to the sequence for last codon in the open reading frame.

[0314](2) Outline of PCR Product

CACC.box-solid..box-solid..box-solid..box-solid..box-solid..box-solid.SacI- /XhoI/

##STR00005##

[0315]cloned into pENTR/D-TOPO to generate pOLE01-MC.box-solid..box-solid..box-solid..box-solid..box-solid..box-soli- d. Oleosin ORF sequenceCACC pENTR/D-TOPO adapter sequenceSacI/XhoI Engineered restriction sites, each site adds 6 base pairs

##STR00006##

Stop Codon

[0316]A map of pOLE01-MC is shown in FIG. 12. The sequence of pOLE01-MC is shown in FIG. 13.

pOLE02-MC

TABLE-US-00013 (3) Primer design (Seq ID No. 3) Forward primer TCTAGAGGTACTXXXXXXXXXXXXXXXXXX (Seq ID No. 4) Reverse primer ACTAGTAGTACCXXXXXXXXXXXXXXXXXX

[0317]In the forward primer XXXX represents an oleosin specific primer that has a 5' end beginning with the first ATG site in the open reading frame.

[0318]In the reverse primer XXXX represents an oleosin specific primer that has a 5' end complementary to the sequence for last codon in the open reading frame.

Outline of PCR Product

[0319]XbaI/GGTACT.box-solid..box-solid..box-solid..box-solid..box-solid..b- ox-solid.GGTACT/SpeI cloned into pCR2.1-TOPO to generate pOLE02-MC.box-solid..box-solid..box-solid..box-solid..box-solid..box-soli- d. Oleosin ORF sequenceGGTACT Extra bases to code for glycine and threonine.

[0320]A map of pOLE02-MC is shown in FIG. 14. The sequence of pOLE02-MC is shown in FIG. 15.

pOLE03-MC

TABLE-US-00014 Primer design (Seq ID No. 5) Forward primer CCCGGGGGTACTXXXXXXXXXXXXXXXXXX (Seq ID No. 6) Reverse primer CTGCAGAGTACCXXXXXXXXXXXXXXXXXX

[0321]In the forward primer XXXX represents an oleosin specific primer that has a 5' end beginning with the first ATG site in the open reading frame.

[0322]In the reverse primer XXXX represents an oleosin specific primer that has a 5' end complementary to the sequence for last codon in the open reading frame.

Outline of PCR Product

[0323]SmaI/GGTACT.box-solid..box-solid..box-solid..box-solid..box-solid..b- ox-solid.GGTACT/PstI cloned into PCR2.1-TOPO to generate pOLE03-MC.box-solid..box-solid..box-solid..box-solid..box-solid..box-soli- d. Oleosin ORF sequenceGGTACT Extra bases to code for glycine and threonine

[0324]A map of pOLE03-MC is shown in FIG. 16. The sequence of pOLE03-MC is shown in FIG. 17.

pOLE04-MC

TABLE-US-00015 (4) Primer design (Seq ID No. 7) Forward primer AAGCTTGGTACTXXXXXXXXXXXXXXXXXX (Seq ID No. 8) Reverse primer ATCGATAGTACCXXXXXXXXXXXXXXXXXX

[0325]In the forward primer XXXX represents an oleosin specific primer that has a 5' end beginning with the first ATG site in the open reading frame.

[0326]In the reverse primer XXXX represents an oleosin specific primer that has a 5' end complementary to the sequence for last codon in the open reading frame.

Outline of PCR Product

[0327]HindIII/GGTACT.box-solid..box-solid..box-solid..box-solid..box-solid- ..box-solid.GGTACT/Bsp1061 cloned into pCR2.1-TOPO to generate pOLE04-MC

.box-solid..box-solid..box-solid..box-solid..box-solid..box-solid. Oleosin ORF sequenceGGTACT Extra bases to code for glycine and threonine

[0328]A map of pOLE04-MC is shown in FIG. 18. The sequence of pOLE04-MC is shown in FIG. 19.

pOLE05-MC

TABLE-US-00016 (5) Primer design (Seq ID No. 9) Forward primer GTCGACGGTACTTCTXXXXXXXXXXXXXXXXXX (Seq ID No. 10) Reverse primer CTCGAGXXXXXXXXXXXXXXXXXX

[0329]In the forward primer XXXX represents an oleosin specific primer that has a 5' end beginning with the first ATG site in the open reading frame.

[0330]In the reverse primer XXXX represents an oleosin specific primer that has a 5' end complementary to the sequence for last codon in the open reading frame.

Outline of PCR Product

[0331]SalI/GGTACTTCT.box-solid..box-solid..box-solid..box-solid..box-solid- ..box-solid.XhoI cloned into pCR2.1-TOPO to generate pOLE05-MC

.box-solid..box-solid..box-solid..box-solid..box-solid..box-solid. Oleosin ORF sequenceGGTACTTCT Extra bases to code for glycine, threonine and serine

[0332]A map of pOLE05-MC is shown in FIG. 20. The sequence of pOLE05-MC is shown in FIG. 21.

pOLE06-MC

[0333]pOLE01-MC and pBLUESCRIPT were digested using SacI and XhoI. The pBLUESCRIPT fragment was ligated into the open pOLE01-MC vector to form pOLE06-MC (FIG. 22). The sequence of pOLE06-MC is shown in FIG. 23.

CACC.box-solid.SacI/.cndot..cndot..cndot..cndot..cndot..cndot./XbaI/SpeI/B- amHI/SmaI/PstI/EcoRI/EcoRV/HindIII/Bsp106/.cndot./SalI/XhoI/

##STR00007##

[0334]CACC pENTR/D-TOPO adapter sequence.box-solid. Oleosin ORF sequenceSacI to XhoI Restriction sites within pBLUESCRIPT.cndot. amino acids encoded within the MCS but not corresponding to a restriction site

##STR00008##

Stop Codon

[0335]Confirmation of the addition of the polylinker was carried out via digestion with SacI, XhoI, XbaI, BamHI, SmaI, PstI, EcoRI, HindIII and SalI. The pOLE06-MC cassette was then sequenced.

pOLE07-MC

[0336]pOLE06-MC was digested using XbaI and pOLE02-MC was digested with XbaI and SpeI, the resulting fragments were ligated together to form pOLE07-MC (FIG. 24). The sequence of pOLE07-MC is shown in FIG. 25.

CACC.box-solid.SacI/.cndot..cndot..cndot..cndot..cndot..cndot./XbaI/.cndot- ..cndot./.box-solid./.cndot..cndot./SpeI/BamHI/SmaI/PstI/EcoRI/EcoRV/HindI- II/Bsp106I/.cndot./SalI/XhoI/

##STR00009##

[0337]CACC pENTR/D-TOPO adapter sequence.box-solid. Oleosin ORF sequencesSpeI to XhoI Restriction sites within pBLUESCRIPT.cndot. amino acids encoded within the MCS but not corresponding to a restriction site

##STR00010##

Stop Codon

[0338]Confirmation of the generation of pOLE07-MC was carried via XbaI/EcoRI, PstI, and HindIII/PstI digests. In order to gain a complete sequence of the clone, an LR reaction was performed to transfer the pOLE07-MC cassette into pET-DEST42. The pOLE07-MC cassette was then sequenced.

pOLE08-MC

[0339]pOLE07-MC and pOLE03-MC were digested using SmaI and PstI, then the required fragments were ligated together to form pOLE08-MC (FIG. 26). The sequence of pOLE08-MC is shown in FIG. 27.

CACC.box-solid.SacI/.cndot..cndot..cndot..cndot..cndot..cndot./XbaI/.cndot- ..cndot./.box-solid./.cndot..cndot./SpeI/BamHI/SmaI/.cndot..cndot./.box-so- lid./.cndot..cndot./PstI/EcoRI/EcoRV/HindIII/Bsp106I/.cndot./SalI/XhoI/

##STR00011##

[0340]CACC pENTR/D-TOPO adapter sequence.box-solid. Oleosin ORF sequencesPstI to XhoI Restriction sites within pBLUESCRIPT.cndot. amino acids encoded within the MCS but not corresponding to a restriction site

##STR00012##

Stop Codon

[0341]Confirmation of the generation of pOLE08-MC was carried out via PstI/NcoI, NotI/XhoI and BamHI digests. In order to gain a complete sequence of the clone, the pOLE08-MC oleosin cassette was transferred into pET-DEST42 by an LR reaction. The cassette was then sequenced and the sequence of the polylinker, and the pOLE03-MC oleosin fragment ligated into pOLE07-MC.

pOLE09-MC

[0342]pOLE08-MC containing the oleosin trimer, was digested using HindIII and ClaI (ClaI is an isoschizomer of Bsp106I), and pOLE04-MC was digested with HindIII and ClaI (Table 1), the resulting fragments were gel purified (FIG. 28). The digests were purified from the agarose gel using the QIAGEN QIAquick Gel Extraction Kit. The HindIII/ClaI digested oleosin isolated from pOLE04-MC was then cloned into the HindIII/ClaI linearised pOLE08-MC vector (table 2) to generate pOLE09-MC (FIG. 29).

[0343]CACC.box-solid.SacI/.cndot..cndot..cndot..cndot..cndot..cndot./XbaI/- .cndot..cndot./.box-solid./.cndot..cndot./SpeI/BamHI/SmaI/.cndot..cndot./.- box-solid./.cndot..cndot.PstI/EcoRI/EcoRV/HindIII/.cndot..cndot./.box-soli- d./.cndot..cndot.ClaI/.cndot./SalI/XhoI/

##STR00013##

CACC pENTR/D-TOPO adapter sequence.box-solid. Oleosin ORF sequencesClaI to XhoI Restriction sites within pBLUESCRIPT.cndot. amino acids encoded within the MCS but not corresponding to a restriction site

##STR00014##

Stop Codon

TABLE-US-00017 [0344]TABLE 1 Table describing the components used in the restriction enzyme digest to produce the linearised pOLE08-MC vector and the oleosin insert/fragment from pOLE04-MC 4 8 10 .mu.L pOLE04-MC 10 .mu.L pOLE08-MC 1 1 .mu.L HindIII (Roche) 1 1 .mu.L ClaI (Roche) 2 2 .mu.L Buffer B (Roche) 6 6 .mu.L sH.sub.2O 20 20 .mu.L Total volume After 2.5 h at 37.degree. C. added 1 1 .mu.L Phosphatase (Roche, CAP, 20 U/uL) Incubated for a further 30 min at 37.degree. C.

TABLE-US-00018 TABLE 2 Table describing the components used in the ligation of the linearised pOLE08-MC vector and the oleosin insert/fragment from pOLE04-MC to produce pOLE09-MC. Ct8 Ct4 1:1 1:3 1:6 3.5 3.5 3.5 3.5 .mu.L pOLE08-MC HindIII/ClaI linearised vector 8 2 6 12 .mu.L Oleosin HindIII/ClaI fragment from 4 4 4 4 4 .mu.L Ligase buffer 1 1 1 1 1 .mu.L T4 DNA Ligase (Roche) 11.5 7 9.5 5.5 .mu.L sH.sub.20 20 20 20 20 20.5 .mu.L Total volume Incubated at 11.degree. C. overnight.

[0345]5 .mu.L of each of the above ligation reactions were then transformed into E. coli DH5.alpha. to allow screening for correct pOLE09-MC plasmids.

[0346]Confirmation of the generation of pOLE09-MC was carried via agarose gel/ethidium bromide analysis of the NcoI/XhoI, NcoI/SpeI/XhoI, XhoI, and NotI/XhoI digests (FIG. 30).

[0347]In order to gain a complete sequence of the clone, the pOLE09-MC oleosin cassette was transferred into pET-DEST42 by an LR reaction. The cassette was then sequenced (FIG. 31).

pOLE10-MC

[0348]Due to poor restriction enzyme digestion efficiency when digesting the oleosin tetramer pOLE09-MC with SalI, pOLE09-M was digested using only XhoI (Table 3). SalI generated ends that are compatible with XhoI generated ends and thereby the SalI/XhoI generated fragment was ligated into the XhoI linearised vector. pOLE05-MC was digested with SalI and XhoI and the resulting oleosin fragment was ligated with pOLE09-MC (table 3) to form pOLE10-MC (FIG. 32).

[0349]CACC.box-solid.SacI/.cndot..cndot..cndot..cndot..cndot..cndot./XbaI/- .cndot..cndot./.box-solid./.cndot..cndot./SpeI/BamHI/SmaI/.cndot..cndot./.- box-solid./.cndot..cndot.PstI/EcoRI/EcoRV/HindIII/.cndot..cndot./.box-soli- d./.cndot..cndot.ClaI/.cndot./SalI/.cndot..cndot./.box-solid.XhoI/

##STR00015##

CACC pENTR/D-TOPO adapter sequence.box-solid. Oleosin ORF sequencesClaI to XhoI Restriction sites within pBLUESCRIPT.cndot. amino acids encoded within the MCS but not corresponding to a restriction site

##STR00016##

Stop Codon

TABLE-US-00019 [0350]TABLE 3 Table describing the components used in the restriction enzyme digest to produce the linearised oleosin tetramer pOLE09-MC vector and the oleosin insert/fragment from pOLE05-MC. 5 9 x3 x2 6 .mu.L pOLE05-MC (midipreped DNA) 6 .mu.L pOLE09-MC (midipreped DNA) 1 2 .mu.L XhoI (Roche) 1 x .mu.L SalI (Roche) 2 2 .mu.L Buffer H (Roche) 10 10 .mu.L sH.sub.2O 20 20 .mu.L Total volume After 2.5 h at 37.degree. C. added -- 1 .mu.L Phosphatase (Roche, CAP, 20U/uL) Incubated for a further 30 min at 37.degree. C.

[0351]The digests were purified from the agarose gel using the QIAGEN QIAquick Gel Extraction Kit. The XhoI/SalI digested oleosin isolated from pOLE05-MC was then cloned into the XhoI linearised pOLE09-MC vector (Table 4) to generate pOLE10-MC.

TABLE-US-00020 TABLE 4 Table describing the components used in the ligation of the linearised pOLE09-MC vector and the oleosin insert/fragment from pOLE05-MC to produce pOLE10-MC. Ct9 Ct5 1:3 1:9 3 6 3 3 .mu.L pOLE09-MC XhoI/Sa/I linearised vector 3 9 .mu.L Oleosin XhoI/Sa/I fragment from pOLE05-MC 1 1 1 1 .mu.L Ligase buffer 4 4 4 4 .mu.L T4 DNA Ligase (Roche) 12 9 9 3 .mu.L sH.sub.20 20 20 20 20.5 .mu.L Total volume Incubated at 11.degree. C. overnight.

[0352]5 .mu.L of each of the above ligation reactions were then transformed into E. coli DH5.alpha. to allow screening for correct pOLE10-MC plasmids. Confirmation of the generation of pOLE10-MC was carried via PstI/XhoI, PstI and SalI/PstI restriction enzyme digests. One clone was selected for detailed agarose/ethidium bromide gel analysis, and compared to pOLE09-MC digested with the same enzymes (FIG. 33).

[0353]In order to gain a complete sequence of the clone, the pOLE10-MC oleosin cassette was transferred into pET-DEST42 by an LR reaction. The cassette was then sequenced (FIG. 34).

Generation of Binary Constructs

[0354]Clones pOLE06-MC through to pOLE10-MC were generated as GATEWAY.TM. entry vectors. The following is a description of subsequent LR reactions performed to transfer the oleosin constructs into two plant binary vectors, pRSh1 (Table 5 and FIG. 35) and pRS12 (Table 5 and FIG. 36).

TABLE-US-00021 TABLE 5 Table describing the components between the left and right borders of two plant binary vectors used to transform the multimeric oleosin repeats into plants. Bacterial Plant Construct Plasmid Cassette Selectable Selectable Name Type Design Marker Marker pRSh1 Plant binary CaMV35s::attR1::GW::attR2::OCS3' Spectinomycin.sup.r BASTA.sup.r pRS12 Plant binary CaMV35s::attR1::GW::attR2::OCS3' Spectinomycin.sup.r Kanamycin.sup.r & GFP expression Key: attR1 GATEWAY .TM. recombination site attR2 GATEWAY .TM. recombination site CaMV35s Cauliflower mosaic virus promoter sequence GFP Jelly Fish Green Fluoresence Protein sequence GW GATEWAY .TM. destination cassette OCS3' Octapine Synthase Terminator sequence

Overview of Experimental Approaches Used to Clone White Clover Oleosin Repeats and DGAT1 into pRSH1.

Linerasing the Entry Clones

[0355]When cloning into pRSH1, linearising the entry clone seemed to make the reaction more efficient. 2 .mu.g of each of the six constructs were digested in 20 .mu.L volumes with the enzyme Alw441 (Roche) which cuts once in the back bone of PENTRD.TM.. Digests were cleaned up using the QIAGEN QIAquick PCR Purification Kit..TM..

[0356]LR reactions were set up between pRSH1 with pOLE06-MC to pOLE10-MC as well as with DGAT1 as per Table 6.

TABLE-US-00022 TABLE 6 LR reactions for cloning oleosin repeats and DGAT1 into pRSH1. Rxn 1 Rxn 2 Rxn 3 Rxn 4 Rxn 5 Rxn 6 Component C6 C7 C8 C9 C10 DGAT1 Linear entry 5.55 5.55 5.55 5.55 5.55 5.55 clone pRSH1 0.2 0.2 0.2 0.2 0.2 0.2 (1.5 .mu.g/.mu.L) LR Clonase .TM. 2 2 2 2 2 2 (.mu.L) LR Rxn 2 2 2 2 2 2 mix .TM. (.mu.L) Topoisomerase 0.25 0.25 0.25 0.25 0.25 0.25 (.mu.L) H.sub.2O (.mu.L) -- -- -- -- -- -- Total (.mu.L): 10 10 10 10 10 10 C6 = pOLE06-MC etc.

[0357]The LR reactions were incubated overnight at 25.degree. C., and were then transformed into E. coli DH5.alpha.. Four colonies were picked for each of the constructs C6-pRSH1, C7-pRSH1, C9-pRSH1 & C10-pRSH1, eight colonies were picked for C8-pRSH1 and three colonies for DGAT1-pRSH1.

Restriction Enzyme Digests to Screen Colonies

[0358]Plasmid DNA was extracted from clones, and purified plasmid was analysed by restriction digest using the following protocol:

TABLE-US-00023 .mu.L Component 2 Plasmid DNA (construct in pRSH1) 1 EcoRI (Roche) 2 Buffer H (Roche) 15 sH.sub.2O 20 Total volume

[0359]Incubated at 37.degree. C. for 2 hours.

[0360]Digests were analysed by agarose/ethidium bromide gel electrophoresis and are shown in FIGS. 37-39.

[0361]Due to difficulties distinguishing between the two constructs C9-pRSH1 and C10-pRSH1 with the EcoRI digest clone1 of C9-pRSH1 and clone2 of C10-pRSH1 were digested with BamHI to determine if both constructs were correct. Digests were analysed by agarose/ethidum bromide gel electrophoresis and are shown in FIGS. 40-41.

Overview of Experimental Approaches Used to Clone White Clover Oleosin Repeats and DGAT1 into pRS12.

Linearising the Binary Plasmid

[0362]When cloning into pRS12, linearising the binary plasmid rather than the entry clone seemed to make the reaction more efficient. 2 .mu.g of pRS12 was digested in a 20 .mu.L reaction volume with the enzyme SmaI (Roche), which makes a single cut between the GATEWAY.TM. att recombination sites in pRS12. The digest was cleaned up using phenol:chloroform:isoamyl alcohol (25:24:1 v/v) and then chloroform. 100% recovery of DNA was assumed from this cleanup method.

[0363]LR reactions were set up between pRS12 with pOLE06-MC to pOLE10-MC as well as with DGAT1 as per Table 7.

TABLE-US-00024 TABLE 7 For LR cloning oleosin repeats and DGAT1 into pRS12. Rxn 1 Rxn 2 Rxn 3 Rxn 4 Rxn 5 Rxn 6 Component C6 C7 C8 C9 C10 DGAT1 Linear entry 1 1 1 1 1 1 clone pRS12 0.2 0.2 0.2 0.2 0.2 0.2 (2 .mu.g/.mu.L) LR Clonase .TM. 2 2 2 2 2 2 (.mu.L) LR Rxn 2 2 2 2 2 2 mix .TM. (.mu.L) Topoisomerase 0.25 0.25 0.25 0.25 0.25 0.25 H.sub.2O (.mu.L) 5.3 5.3 5.3 5.3 5.3 5.3 Total (.mu.L): 10 10 10 10 10 10 C6 = pOLE06-MC etc.

[0364]The LR reactions were incubated overnight at 25.degree. C., and were then transformed into E. coli DH5.alpha.. Twelve colonies were picked for analysis from the C6-pRS12 construct, two colonies from C7-pRS12, two from C8-pRS12, three from C9-pRS12, three from C10-pRS12, and two from DGAT1-pRS12.

Restriction Enzyme Digests to Screen Colonies

[0365]Plasmid DNA was extracted from clones, and purified plasmid was analysed by restriction digest using the following protocol:

TABLE-US-00025 .mu.L Component 2 Plasmid DNA (construct in pRS12) 1 Restriction enzyme (Roche) 2 Buffer (Roche) 15 sH.sub.2O 20 Total volume

[0366]Incubated at 37.degree. C. for 2 hours.

[0367]Digests were analysed by agarose/ethidium bromide gel electrophoresis and are shown in FIGS. 42-45.

[0368]Representative maps of a pRSH1 binary vector containing white clover oleosin multimers is shown in FIG. 46.

[0369]Representative maps of a pRS12 binary vector containing white clover oleosin multimers is shown in FIG. 47.

Generation of Polyclonal Antibodies to White Clover Oleosin

[0370]Cloning of N-Terminal Region of White Clover Oleosin Into the pDEST17 and pET-DEST42 Expression Vectors

[0371]The N-terminal region of oleosin was cloned into the pENTR-D vector, to produce the construct pEON. The N-terminal region of oleosin was transferred into the pDEST17 and pET-DEST42 vectors (Invitrogen) by the LR reaction to produce the constructs p17NON (FIG. 48) and p42CON (FIG. 49), which were then transformed into E. coli DH5.alpha.. p17NON was designed to express the N-terminal oleosin peptide with an N-terminal 6.times.His tag (6HON). The p42CON was designed to express the N-terminal oleosin peptides with a C-terminal 6.times.His tag (ON6H).

[0372]Plasmid DNA purified from the putative constructs was analysed by PCR using T7 and T7t primers (as marked on the maps in FIG. 48 and FIG. 49), to determine if the terminal regions were present (FIG. 50 and FIG. 51).

[0373]Plasmid DNA from lines p42CON-2 and p17NON-1 were transformed into E. coli strains BL21 and BL21-Al for protein expression.

[0374](b) Sequence Analysis of Putative p17NON and p42CON

[0375]The p17NON and p42CON plasmid lines were sequenced from the 5' and 3' ends using T7 and T7t primers, respectively. The sequences obtained showed that the N-terminal regions of oleosin had been cloned in frame into both the pDEST17 and pET-DEST42 vectors.

Expression of Tagged Peptides

Example of Standard Culture and Induction Protocol

[0376]10 mL LB Amp100 broths were inoculated with expression construct in E. coli BL21-AI and incubated overnight at 37.degree. C. 220 rpm. The next day duplicate 10 mL LB Amp100 broths were inoculated with 500 .mu.L of the overnight cultures (to give OD.sub.600=0.05-0.1). All cultures were incubated for approximately three hours at 37.degree. C. 220 rpm, until OD.sub.600=0.5-0.7 was reached. One set of the duplicate cultures was induced by the addition of 20% Arabinose to a final concentration of 0.2% and IPTG (isopropyl .beta.-D-thiogalactopyranoside) to a final concentration of 1 mM. The second set of duplicate cultures was used as the non-induced negative controls, and therefore nothing was added to these cultures. All cultures were then incubated overnight at 37.degree. C. 220 rpm. 1 mL aliquots were removed from each culture and prepared for SDS-PAGE analysis (Table 8).

TABLE-US-00026 TABLE 8 Standard prokaryotic induction protocol. 1.degree. broth 10 mL LB Amp100 broths 1.degree. inoculation Colony picked from plate by toothpick 1.degree. incubation Overnight at 37.degree. C. 220 rpm conditions 2.degree. broth 10 mL LB Amp100 broths (in duplicate) 2.degree. inoculation 500 .mu.L of the overnight cultures (to give OD600 = 0.05-0.1) 2.degree. incubation Approximately three hours at 37.degree. C. 220 rpm, until OD600 = 0.5-0.7 conditions Induction +ve - 20% Arabinose to a final concentration of 0.2% and IPTG (isopropyl .beta.-D-thiogalactopyranoside) to a final concentration of 1 mM -ve - nothing added to non-induced negative control cultures Induction incubation Overnight at 37.degree. C. 220 rpm conditions Additional This may include harvesting and lysing cells preparation Analysis 1 mL aliquots were removed from each culture and prepared for SDS-PAGE analysis

[0377]Purification of Tagged White Clover Oleosin Peptides

[0378]HIS-Select Nickel Affinity Gel (Sigma) was used to purify the oleosin 6.times.HIS tagged proteins under denaturing conditions (Table 9 shows the buffers used).

Denaturing Buffers

TABLE-US-00027 [0379]TABLE 9 Buffers used to purify tagged white clover oleosin. Final vol. (mL) Final 100 100 100 Stock conc EQUIL'N WASH ELUTION (M) (M) BUFFER BUFFER BUFFER PO mL 0.25 0.1 40 40 40 Urea g 6 36 g 36 g 36 g (Mr = 60.06) NaCl mL 5 0.3 6 6 6 Imidazole mL 2 0.005 0.25 Imidazole mL 2 0.02 1 Imidazole mL 2 0.25 12.5 pH 5M HCl 8.0 8.0 8.0

Example of Standard Large Scale Purification Protocol

[0380]1.5 mL of HIS-Select Nickel Affinity Gel was transferred to a chromatography column. The affinity gel was washed with two volumes of deionized water and then equilibrated with three volumes of equilibration buffer. The clarified crude extract was loaded onto the column at a flow rate of 2 to 10 column volumes/hour. After the extract was loaded, the column was washed with wash buffer at a flow rate of about 10 to 20 column volumes/hour. The 6.times.His tagged protein was eluted from the column using 3 to 10 column volumes of elution buffer at a flow rate of 2 to 10 column volumes/hour. Fractions were collected continuously and assayed for the target protein using Bradford's protein assay.

N-Terminal Fragment of White Clover Oleosin

[0381]Induction of p17NON and the Expression of 6HON (Oleosin N-Terminal with N-6.times.His tag)

TABLE-US-00028 TABLE 10 Large scale induction protocol. 1.degree. broth 10 mL LB Amp100 broths 1.degree. inoculation p17NON in E. coli BL21-Al, colony picked from plate by toothpick 1.degree. incubation Overnight at 37.degree. C. 220 rpm conditions 2.degree. broth 10 mL LB Amp100 broths 2.degree. inoculation 500 .mu.L of the overnight cultures (to give OD600 = 0.05-0.1) 2.degree. incubation Approximately three hours at 37.degree. C. 220 rpm, until OD600 = 0.5-0.7 conditions Induction 20% Arabinose to a final concentration of 0.2% and IPTG (isopropyl .beta.-D-thiogalactopyranoside) to a final concentration of 1 mM Induction incubation Overnight at 37.degree. C. 220 rpm conditions Analysis 1 mL aliquots were removed from each culture and prepared for SDS-PAGE analysis (FIG. 52)

Inclusion Body Preparation of 6HON For Purification

TABLE-US-00029 [0382]TABLE 11 Inclusion body preparation for E. coli expressed white clover oleosin. 1.degree. broth 5 mL LB Amp100 broths 1.degree. inoculation p17NON in E. coli BL21-AI 1.degree. incubation Overnight at 37.degree. C. 220 rpm conditions 2.degree. broth 50 mL LB Amp100 broths 2.degree. inoculation 3.5 mL of the overnight cultures (to give OD600 = 0.05-0.1) 2.degree. incubation Approximately three hours at 37.degree. C. 220 rpm, until OD600 = 0.5-0.7 conditions Induction 20% Arabinose to a final concentration of 0.2% and IPTG (isopropyl .beta.-D-thiogalactopyranoside) to a final concentration of 1 mM Induction incubation Overnight at 37.degree. C. 220 rpm conditions Additional The induced cells were collected by centrifugation and resuspended in preparation 1/10 culture volume of buffer (50 mM Tris-HCl pH 8.0, 2 mM EDTA). Lysozyme was added to a concentration of 100 .mu.g/mL, 1/10 volume of 1% Triton X-100 was then added, mixed gently and incubated at 30.degree. C. for 15 minutes. DNA was sheared by sonication and the insoluble protein fraction was separated from the soluble fraction by centrifugation. Analysis 1 mL aliquots were removed from each culture and prepared for SDS-PAGE analysis (FIG. 53)

Nickel Affinity Chromatography to Purify 6HON

[0383]HIS-Select Nickel Affinity Gel (Sigma) was used to purify the 6HON under denaturing conditions (as described above).

[0384]A trial scale purification of 6HON was carried out using a 2 mL sample from the insoluble protein fraction (as described above). The isolated 6HON was visualised using SDS-PAGE (FIG. 54).

Large Scale Purification of 6HON

TABLE-US-00030 [0385]TABLE 12 Large scale preparation for prokaryotically produced white clover oleosin for antibody generation. 1.degree. broth 5 mL LB Amp100 broths 1.degree. inoculation p17NON in E. coli BL21-AI 1.degree. incubation Overnight at 37.degree. C. 220 rpm conditions 2.degree. broth 500 mL LB Amp100 broths 2.degree. inoculation 50 mL of the overnight cultures (to give OD600 = 0.05-0.1) 2.degree. incubation Approximately three hours at 37.degree. C. 220 rpm, until OD600 = 0.5-0.7 conditions Induction 20% Arabinose to a final concentration of 0.2% and IPTG (isopropyl .beta.-D-thiogalactopyranoside) to a final concentration of 1 mM Induction incubation Overnight at 37.degree. C. 220 rpm conditions Additional The induced cells were collected by centrifugation and resuspended in preparation 1/10 culture volume of buffer (50 mM Tris-HCl pH 8.0, 2 mM EDTA). Lysozyme was added to a concentration of 100 .mu.g/mL, 1/10 volume of 1% Triton X-100 was then added, mixed gently and incubated at 30.degree. C. for 15 minutes. DNA was sheared by sonication and the insoluble protein fraction was separated from the soluble fraction by centrifugation. Analysis 1 mL aliquots were removed from each culture and prepared for SDS-PAGE analysis

[0386]HIS-Select Nickel Affinity Gel was used to purify 6HON under denaturing conditions (as described above). A large scale purification of 6HON was carried out using the 500 mL sample (induced as described above). The purified 6HON was visualised using SDS-PAGE (FIG. 55) and the concentration of the eluted protein was estimated using a Bradford's protein assay, and found to be approximately 0.72, 2.74 and 1.89 mg/mL, for Elutions 1, 2 and 3 respectively (FIG. 56).

Generation of Rabbit Anti-White Clover Oleosin Antisera

Immunisation of Rabbit

[0387]66 .mu.L of Elution 2 (see Large scale purification of 6HON, above), containing 250 .mu.g purified protein, was mixed with 433 .mu.L PBS. This was passed to the Massey University Small Animals Unit for immunisation of a rabbit (male, ID# 124, Massey University Animal Ethics Committee (MUAEC) approval number 04/28). 25 days after the primary immunisation the first boost was administered (66 .mu.L of Elution 2, containing 250 .mu.g purified protein, mixed with 433 .mu.L PBS), and the second boost was given 46 days after the primary immunisation (128 .mu.L of Elution 1, containing 250 .mu.g purified protein, mixed with 372 .mu.L PBS).

Preparation of Rabbit Anti-White Clover Oleosin Antisera

[0388]53 days after the primary immunisation approximately 3 mL of blood was taken from the rabbit and placed at 4.degree. C. for approximately 16 h. To separate the serum the blood was centrifuged at 1500.times.g 20 min 4.degree. C. The serum (1.5 mL) was transferred to a fresh tube and stabilised with 0.25% Phenol in PBS and 0.01% Methiolate.

Assaying Titre and Specificity of Rabbit Anti-White Clover Oleosin Antisera by SDS-PAGE Immunoblot Analysis

[0389]The samples outlined in Table 13 were analysed by SDS-PAGE immunoblot analysis using the anti oleosin N terminal antibody (FIG. 57).

TABLE-US-00031 TABLE 13 Samples used to determine titre and specificity of polyclonal rabbit anti-white clover oleosin antisera. Lane ID Load Oleosin Induced Expressed 1 FLA-BL21_AI, E. coli 1 .mu.L 6HOF - - 2 FLA-BL21_AI, E. coli 1 .mu.L 6HOF + + 3 17C-2-BL21_AI, E. coli 1 .mu.L 6HOC + + 4 Elu1, 1:200, pure 1 .mu.L 6HON, 1.8 ng + + 5 Elu2, 1:200, pure 1 .mu.L 6HON, 6.9 ng + + 6 Elu3, 1:200, pure 1 .mu.L 6HON, 4.7 ng + + 8 clover seed extract 0.1 .mu.L 1.6 .mu.g total protein 9 clover seed extract 1 .mu.L 16 .mu.g total protein 10 clover seed extract 5 .mu.L 80 .mu.g total protein

Using Rabbit Anti-White Clover Oleosin Antisera to Detect Oleosin in Clover Seed Oil Bodies

[0390]We checked to see if the antibodies were capable of detecting full-length oleosin. Early analysis of the antibodies on crude clover seed protein extracts had shown that the antibodies were able to be used to detect a protein of the expected size when clover seed oil body extracts were analysed by Immunoblot analysis (FIG. 58).

[0391]Results from the immunoblot showed that the anti-oleosin N-terminal antibodies could be used to specifically detect a .about.20 kDa protein--the expected size of the clover oleosin protein.

Overview of Experimental Approaches Used to Transform Plants with White Clover Polyoleosin Clones.Transformation of Brassica oleracea with White Clover Polyoleosin and DGAT1 Constructs

[0392]A total of 12 constructs were transformed into Brassica oleracea (Table 14. These were all transferred into Agrobacterium tumefaciens strain LBA4404 via the freeze-thaw method described in Christey and Braun (2004). Colonies were selected on LB medium containing 100 ml/l streptomycin and 100 ml/l spectinomycin. PCR analysis for the BAR gene was used to confirm plasmid presence in Agrobacterium colonies.

TABLE-US-00032 TABLE 14 Summary of constructs placed into Brassica oleracea. Construct C&F code Genes Marker pRSH1-C6 AgR 6 35S-oleosin monomer 35S-BAR pRSH1-C7 AgR 7 35S-oleosin dimer 35S-BAR pRSH1-C8 AgR 8 35S-oleosin trimer 35S-BAR pRSH1-C9 AgR 9 35S-oleosin tetramer 35S-BAR pRSH1-C10 AgR 10 35S-oleosin pentamer 35S-BAR pRSH1-At DGAT DGAT 35S-Arab. DGAT 35S-BAR pRSh4 Arab. oleosin seed 35S-BAR promoter + GUSi pRSh6 oleosin seed prom. + 35S-BAR oleosin monomer pRSh7 oleosin seed prom. + 35S-BAR oleosin dimer pRSh8 oleosin seed prom. + 35S-BAR oleosin trimer pRSh9 oleosin seed prom. + 35S-BAR oleosin tetramer pRSh10 oleosin seed prom. + 35S-BAR oleosin pentamer

Plant Material and Transformation

[0393]For these experiments a rapid cycling (RC) B. oleracea line, DH1012, selected for high regeneration and transformation ability by Sparrow et al. (2004) was used. Seeds were germinated in vitro as described in Christey et al. (1997). Hypocotyl and cotyledonary petiole explants from 4-5 day-old seedlings were co-cultivated briefly with a culture of Agrobacterium grown overnight in LB medium containing antibiotics prior to 1:10 dilution in antibiotic-free minimal medium (7.6 mM (NH.sub.4).sub.2SO.sub.4, 1.7 mM sodium citrate, 78.7 mM K.sub.2HPO.sub.4, 0.33M KH.sub.2PO.sub.4, 1 mM MgSO.sub.4, 0.2% sucrose) with growth for a further 4 hrs. Explants were cultured on Murashige-Skoog (MS; Murashige and Skoog, 1962) based medium with B5 vitamins and 2.5 mg/L BA. After 3 days co-cultivation, explants were transferred to the same medium with 300 mg/L Timentin (SmithKline Beecham) and subsequently placed on selection medium with 2.5 mg/L Basta. Green shoots were transferred to hormone-free Linsmaier-Skoog based medium (LS; Linsmaier and Skoog, 1965) containing 5 mg/L Basta and solidified with 10 gm/L Danisco Standard Agar. Explants were cultured in tall Petri dishes (9 cm diameter, 2 cm tall) sealed with Micropore (3M) surgical tape. Shoots were cultured in clear plastic tubs (98 mm, 250 ml, Vertex). All culture manipulations were conducted at 25.degree. C. with a 16 h/day photoperiod, provided by Cool White fluorescent lights (20 .mu.E/m.sup.2/s).

Determination of Selective Levels of Basta

[0394]Hypocotyl and cotyledon explants from 4 day-old seedlings were cultured on LSN medium containing 2.5 mg/L BAP and 300 mg/L Timentin and 5 different levels of Basta (0, 2.5, 5, 10 and 25 mg/L) to determine the appropriate level to use for selection in co-cultivation experiments.

[0395]To determine the selective level of Basta for maintenance of in vitro shoots, small healthy apical cuttings were transferred to tall pots of hormone-free LSn containing either 2.5 or 5 mg/L Basta.

Conformation of Brassica oleracea Transformation by PCR

[0396]DNA was isolated from leaves of in vitro shoots using the rapid method described in Christey and Braun (2004). PCR was conducted to test for the presence of the bar gene using the primers baran (5'-tcagatctcggtgacgggcagg-3') (Seq ID No. 11) and barse (5'-atgagccaagaacgacgcccgg-3') (Seq ID No. 12) to produce a 551 bp product. PCR conditions were: 94.degree. C. for 30 sec, 65.degree. C. for 30 sec and 72.degree. C. for 30 sec over 40 cycles.

[0397]PCR was conducted on Bar positive samples to check for the presence of the oleosin clones using the primers outlined in Table 15. PCR conditions were: 94.degree. C. for 30 s, 45.degree. C. for 30 s and 68.degree. C. for 30 s for 30 cycles. A 650 bp product was expected.

TABLE-US-00033 TABLE 15 Primers used for oleosin PCR. Primer name Sequence Sequence IDs AgR 6 forward CACCATGGCACAACCT SEQUENCE ID NO. 13 CAAGTT AgR 7 forward GCTCCACCGCG SEQUENCE ID NO. 14 AgR 6/7 reverse TCCACTAGTTCTAG SEQUENCE ID NO. 15 AgR 8 forward CTAGAACTAGTGGAT SEQUENCE ID NO. 16 AgR 8 reverse TCCTGCAGAGTAC SEQUENCE ID NO. 17 AgR 9 forward GTACTCTGCAGGA SEQUENCE ID NO.18 AgR 9 reverse ATACGATAGTAC SEQUENCE ID NO. 19 AgR 10 forward CTATCGATACCGTCG SEQUENCE ID NO. 20 AgR 10 reverse CTCGAGTGTTGATCTC SEQUENCE ID NO. 21 TTAGCTTC

Conformation of White Clover Polyoleosin Construct Gene Expression in Brassica oleracea Transformants by RT-PCR

[0398]RNA was isolated from plants using the Concert.TM. small scale isolation reagent (Invitrogen). DNA was digested using Turbo DNase (Ambion). For RT-PCR the primers described in Table 15 were used to amplify the transcribed region. Reactions were performed on RNA samples using the Superscript.TM. III (Invitrogen) Reverse Transcriptase, with the RT step performed at 50.degree. C. followed by PCR.

Agrobacterium Transformation

[0399]PCR for the Bar gene was used to confirm the presence of the oleosin-containing plasmids in Agrobacterium colonies (FIG. 59). Two BAR positive colonies from each transformation event were selected for storage at -80.degree. C. in glyercols and used in subsequent explant co-cultivation experiments.

Determination of Selective Levels of Basta

[0400]The results of the explant selection experiment confirmed that use of 2.5 mg/L Basta was suitable for use as the selection level for subsequent co-cultivation experiments. After 2-4 weeks on this level rare shoot regeneration was noted (FIG. 60). In contrast, in vitro shoot cuttings showed some development on 2.5 mg/L Basta with root development apparent on some. In contrast, after 4-5 weeks on 5 mg/L Basta cuttings turned brown with no root development. This level was used in subsequent experiments for growth of putative transgenic shoots.

Selection of Transgenic Shoots

[0401]At least 150 explants were co-cultivated with each construct (Table 16). Three to four weeks after co-cultivation rare small green shoots were apparent. Putative Basta resistant shoots were excised and transferred to hormone-free media containing 5 mg/L Basta. In vitro shoot and root growth on Basta-containing medium confirmed plants were transgenic. Transgenic plants were healthy with good shoot and root development and normal phenotype. In contrast, Basta sensitive cuttings showed little development (FIG. 61). Transgenic shoots were obtained mainly from hypocotyl explants with only rare transgenic shoots obtained from cotyledon explants. While the overall transformation rate was only 1.2%, there was a lot of variation between both experiments and explants, with some combinations producing over 5% transformation in some experiments.

TABLE-US-00034 TABLE 16 Summary of PCR positive shoots. No. explants No. PCR + cocultivated ve for BAR Construct cotyledon hypocotyl cotyledon hypocotyl Total pRSH1-C6 70 90 0 6 6 pRSH1-C7 170 110 1 3 4 pRSH1-C8 390 190 2 2 4 pRSH1-C9 390 190 0 4 4 pRSH1-C10 250 120 3 7 10 At DGAT 416 195 0 8 8 pRSh4 200 120 2 2 4 pRSh6 100 50 0 0 0 pRSh7 110 30 0 1 1 pRSh8 110 50 1 2 3 pRSh9 110 50 0 0 0 pRSh10 110 50 1 0 1 Total 2426 1245 10 35 45

Conformation of Transformation by PCR

[0402]Shoots growing on 5 mg/L Basta that were still green and showing good root development after at least two subcultures had DNA extracted and PCR performed for the bar gene. Over 250 shoots were analysed with 45 confirmed as having the bar gene (20%) (Table 10). PCR analysis confirmed the presence of the Bar gene in all plants that had shown good growth on selective levels of Basta in vitro. PCR for the Bar gene produced a 551 bp fragment (FIG. 62). PCR analysis of Bar positive shoots for the oleosin gene indicated that not all plants contain the oleosin gene as well (FIG. 63).

[0403]Transgenic shoots were obtained for 10 of the 12 constructs in Table 14. Most constructs had at least 4 independent transgenic shoots but no transgenic shoots were obtained for pRSh6 and pRSh9. Negative shoots were retained on 5 mg/L Basta in case they were false negatives and re-tested if they remained green with roots. Generally PCR negative shoots showed Basta sensitivity symptoms in subsequent subculture rounds suggesting negative PCR results were genuine. For all transgenic lines 1-2 pots of clonal cuttings remain in vitro. All lines appeared healthy with good root and shoot development and normal phenotype.

Conformation of Expression by RT-PCR

[0404]RT-PCR analysis confirmed expression of the oleosin construct in 4 out of 5 lines tested (FIG. 64).

Transformation of Lotus japonicus with Agrobacterium rhizogenes Northern Analysis of RNA Extracted from Hairy Roots

[0405]Northern blot analysis was performed on transformed Lotus japonicus hairy roots (see below) to confirm the expression of the polyoleosin constructs. The blot was probed with .sup.32P labeled, random primed, white clover oleosin cDNA (FIG. 65). The Northern blot analysis shows that the constructs are transcribed. In each case it appears that transcription has finished close to the 3' end of the OCS terminator where a single oleosin transcript and the terminator are roughly 1.5 kb in length. It is clear that the transcript from the single oleosin is highly expressed in the majority of the single oleosin transformants. Each additional oleosin repeat resulted in the increase in the transcript size by the appropriate amount (.about.650b). As such that the sizes are as follows 1.4 kb, 2 kb, 2.7 kb, 3.4 kb and 4 kb for the oleosin monomer, dimer, trimer, tetramer and pentamer, respectively. The level of transcript accumulated appears to be inversely proportional to the number of oleosin repeats. Furthermore, the transformants containing either the oleosin monomer or dimer did not have any transcripts of unexpected size hybridising to the oleosin probe, whereas the transformants containing the oleosin trimer, tetramer or pentamer had a number of additional hybridising bands. In the majority of cases the bands were considerably larger than the expected size, frequently >4.4 kb, and in only one case did the hybridising band appear to be smaller than the predicted transcript. Since the extra bands only appear in lines transformed with the trimeric or larger oleosin repeats, we have assumed that these bands represent aberrantly processed oleosin RNA, and in many cases the processing appears to have failed to terminate transcription.

Transformation of Lotus japonicus with Agrobacterium rhizogenes (A4T)

Protocol

Day 1

[0406]Scarify lotus seeds using p220 wet/dry sand paper [0407]Sterilise seeds by rotating for 20 min in 10 mL sterilisation soln: [0408]7 mL 100% ethanol [0409]1 mL 30% H.sub.2O.sub.2 [0410]2 mL H.sub.2O [0411]Wash 3 times in sterile H.sub.2O [0412]Place seeds on 1% water agar plates [0413]Wrap plates in tinfoil (dark) and germinate at 25.degree. C. for 2 days [0414]Streak TY agar plate with Agrobacterium rhizogenes (A4T) glycerol stock and grow overnight @ 28.degree. C.

Day 2

[0414] [0415]Inoculate 50 mL YEB culture broth with colony from A4T plate and grow overnight @ 28.degree. C. shaking (220 rpm)

Day 3

[0415] [0416]Make Agrobacterium competent cells and transform with binary plasmid containing gene of interest, plate on TY agar plates and grow for 2 days at 28.degree. C. (refer: Transformation of Agrobacterium) [0417]Transfer germinated seeds to 1/2 B5 media, approx 10 across each plate, roots pointing down. [0418]Tape plates together, grow vertically on lab bench.

Day 5

[0418] [0419]Pick colonies from Agrobacterium plates into 10 mL TY-spectomycin broths and grow at 28.degree. C. shaking (220 rpm) for 2 days.

Day 6

[0419] [0420]Perform PCR on Agrobacterium broths to check for desired gene.

Day 7

[0420] [0421]Inoculate Lotus japonicus plants by dipping a sterile scalpel into the Agrobacterium broth and cutting off the root. After inoculation tape plates together, wrap in tinfoil and leave overnight on lab bench

Day 8

[0421] [0422]Unwrap plates and grow for 2 days vertically on lab bench

Day 9

[0422] [0423]Transfer plants to MS (CRO) media containing the antibiotic cephotaximine, 10 across a plate. Grow vertically on lab bench. [0424]Roots can be viewed (for GFP) under a Microscope 10-20 days later.

[0425]Media

1/2 B5 Media (No Sucrose)

TABLE-US-00035 0.0425 g NaH.sub.2PO.sub.4.cndot.2H.sub.20 0.625 g KN0.sub.3 0.0335 g (NH.sub.4).sub.2S0.sub.4 0.0625 g MgS0.sub.4.cndot.2H.sub.20 0.01 g Ferric EDTA 0.025 g Myo-Inositol 0.25 mL Stock A 0.25 mL Stock B 0.25 mL Stock C 0.25 mL Stock D

[0426]Adjust pH to 5.5 with 0.2M KOH or 0.2M HC.sub.1-6 [0427]6 g Agar

[0428]Make up to 500 mL with sterile H20

MS(CRO) Media

TABLE-US-00036 [0429]50 mL MS Macro Stock 5 mL MS Macro Stock 5 mL MS Fe (EDTA) Stock 1 mL B5B Vitamins stock 30 g Sucrose 100 mg Myo-Inositol 8 g Phytagel agar pH to 5.7 with NaOH Final volume = 1000 mL

MS Macro Stock

TABLE-US-00037 [0430]33 g NH.sub.4NO.sub.3 38 g KNO.sub.3 8.8 g CaCl.sub.2.cndot.2H.sub.2O 3.4 g KH.sub.2PO.sub.4 7.4 g MgSO.sub.4.cndot.7H.sub.2O Final volume = 1000 mL

MS Fe (EDTA) Stock

TABLE-US-00038 [0431]4 g Ferric EDTA (Fe Na Ethylene diaminetetra acetic) Final volume = 500 mL

MS Micro Stock

TABLE-US-00039 [0432]1.24 g H.sub.3BO.sub.3 4.46 g MnSO.sub.4.cndot.4H.sub.20 1.72 g ZnSO.sub.4.cndot.7H.sub.20 0.166 g KI 0.05 g Na.sub.2MoO.sub.4.cndot.2H.sub.20 0.005 g CuSO.sub.4.cndot.5H.sub.20 0.005 g CoCl.sub.2.cndot.6H.sub.20 Final volume = 1000 mL

B5 Vitamin Stock

TABLE-US-00040 [0433] 0.1 g Nicotinic Acid 1.0 g Thiamine HCl 0.1 g Pyridoxine HCl Final volume = 100 mL 1 mL aliquots into eppendorfs Store at -20.degree. C.

Notes

Transformation of Lotus:

[0434]This protocol includes the transformation of Agrobacterium which sometimes is just being grown from glycerols. Also is written as for GFP--if for PPT resistant plants then on day 9 (or just when roots are visible) we transfer to selective plates. Usually 4 plants (roots only) per plate. Once selection has taken place (either GFP or PPT) individual roots are transferred to individual plates. Supposedly we transfer all or some of the tissue to a new plate each month. Once we are growing root portions only the plates are kept horizontal, sealed and in darkness, usually in the 25 C room.Transformation of Agrobacterium rhizogenes (A4T) [0435]1. Streak a TY agar plate with Agrobacterium rhizogenes (A4T) glycerol stock and grow 28.degree. C. overnight. [0436]2. Inoculate 50 mL of YEB broth with a colony from Agrobacterium plate and grow at 28.degree. C., shaking (220 rpm) until OD.sub.600 is approx 0.5 (16 h) [0437]3. Centrifuge cells for 15 min @ 400 rpm, discard supernatant and resuspend in 10 mL of 0.15M NaC.sub.1-4 [0438]4. Centrifuge cells for 10 min @ 4000 rpm, discard supernatant, and resuspend in 1 mL of ice-cold 20 mM CaCl.sub.2 [0439]5. Aliquot 200 .mu.L of cells into an eppendorf tube, add 5 .mu.g of DNA and incubate on ice for 30 min. [0440]6. With what is left of the 1 mL aliquot 186 .mu.L of cells and 14 .mu.L of DMSO into eppendorf tubes and freeze in liquid N.sub.2 then store at -70.degree. C. [0441]7. After incubation on ice for 30 mins freeze the DNA/cells in liquid N.sub.2 for 1 min. [0442]8. Thaw in a 37.degree. C. waterbath [0443]9. Repeat steps 7 & 8 [0444]10. Add 1 mL of YEB broth and incubate cells for 4 h @ 28.degree. C. with gentle shaking [0445]11. Plate cells on TY agar containing spectomycin and grow for 2 days @ 28.degree. C. [0446]12. Pick colonies from the Agrobacterium plates into 10 mL TY broths containing spectomycin and grow for 2 days @ 28.degree. C., shaking at 220 rpm.

[0447]Agrobacterium transformed with a binary vector are prepared for infiltration by plating or spreading a bacterial lawn on the appropriate plate with appropriate antibiotics (although Rifampicin is not normally included). The Agrobacterium should be grown at 28.degree. C. for 2-3 days.

Clover Seed Oilbody Purification

Buffers for Oilbody Extraction

Buffer A

TABLE-US-00041 [0448]4 mL 500 mM NaPhosphate Buffer, pH 7.5 41.1 g sucrose Final volume = 200 mL (with dH.sub.2O)

Buffer D

TABLE-US-00042 [0449]1 mL 500 mM NaPhosphate Buffer, pH 7.5 17.1 g sucrose 23.4 g NaCl Final volume = 200 mL (with dH.sub.2O)

Detergent Washing Solution

TABLE-US-00043 [0450]0.4 mL 10% Tween 20 (0.1%) 20 mL Floating Buffer (1/2x Buffer D) Final volume = 40 mL (with dH.sub.2O)

[0451]Procedure [0452]1. Weigh 2 g of clover seed. [0453]2. Homogenate the seed in .about.20 mL of Buffer A with sand in a mortar and pestle. [0454]3. Transfer to two 15 mL Falcon tubes and centrifuge 3200.times.g 10 min RT. [0455]4. Transfer upper aqueous phase and any floating material to two 15 mL Falcon tubes and add 1 mL Buffer D. [0456]5. Resuspend the oil bodies thoroughly by sonication Power-1 Duty Cycle-100% 5.times.30 sec. [0457]6. Centrifuge 10,000 rpm 10 min RT. [0458]7. Transfer upper/floating oil-body layer at the top with a bended spatula to 2 mL microfuge tubes containing 1.5 mL of Detergent Washing Solution. [0459]8. Resuspend the oil bodies thoroughly by sonication Power-1 Duty Cycle-100% 5.times.30 sec. [0460]9. Centrifuge 10,000 rpm 10 min RT. [0461]10. Transfer upper/floating oil-body layer at the top with a bended spatula to 2 mL microfuge tubes containing 1.5 mL of Buffer A. [0462]11. Resuspend the oil bodies thoroughly by sonication Power-1 Duty Cycle-100% 5.times.30 sec. [0463]12. Centrifuge 10,000 rpm 10 min RT. [0464]13. Transfer upper/floating oil-body layer at the top with a bended spatula to 2 mL microfuge tubes containing 500 .mu.L of Buffer A. [0465]14. Resuspend the oil bodies thoroughly by vortexing and prepare samples for SDS-PAGE analysis.RNA Isolation from Plants Using the QIAGEN RNeasy Kit

[0466]RNA was isolated from Agrobacterium tumefaciens infected N. benthamiana leaves and Agrobacterium rhizogenes infected L. japonicus roots using the RNeasy Plant Mini Kit (QIAGEN, Hilden, Germany). Approximately 0.1 g of tissue was removed from the plant, placed into a 1.5 mL microcentrifuge tube, frozen in liquid nitrogen and ground to a fine powder using a stainless steel rod. 450 .mu.L RLT Buffer (guanidinium isothiocyanate) and 4.5 .mu.L .beta.-mercaptoethanol were added and the mixture vortexed vigorously until the sample thawed then for a further 30 sec. The lysate was transferred onto a QIAshredder spin column (lilac), fitted in a 2 mL collection tube (supplied) using a 1 mL pipette with the end of the tip cut off to prevent blockages. The mixture was spun in microfuge for 2 min at 13000 rpm. The filtrate was transferred to a 1.5 mL centrifuge tube taking care not to disturb the debris in collection tube. 225 .mu.L Absolute Ethanol (0.5 vols.) was added and mixed immediately by pipetting. The filtrate/ethanol mix, and any precipitate, was decanted onto the RNeasy mini spin column (pink) which had been fitted in a 2 mL collection tube (supplied). The mixture was spun in a microfuge for 15 sec at 13000 rpm. The filtrate was then discarded, but the column and collection tube were retained for the next step. To column was washed by loading on 700 .mu.L RW1 Buffer then spun in a microfuge for 15 sec at 13000 rpm. The filtrate was discarded, and 500 .mu.L RPE Buffer was loaded onto the column, which was then spun in a microfuge for 15 sec at 13000 rpm. Again, the filtrate was discarded and another 500 .mu.L RPE Buffer was loaded onto the column and spun for 15 sec at 13000 rpm. The filtrate was discarded, and the column was spun for an additional min at 13000 rpm to thoroughly dry the column. Next the column was carefully removed from the collection tube, avoiding the carry-over of ethanol/wash buffer. The RNeasy column was then placed into a fresh 1.5 mL collection tube (supplied) and 30 .mu.L RNase-free H.sub.2O was added onto the column. The column was spun in a microfuge for 60 sec at 13000 rpm to elute the RNA. The RNA was stored at -20.degree. C. until required.

RT-PCR

[0467]cDNA synthesis.

[0468]Expand Reverse Transcriptase, Roche, cat#1785826, supplied with 5.times. Buffer and DTT.

TABLE-US-00044 8.5-9.5 .mu.L Total RNA (1 .mu.g recommended) either 2 .mu.L 10 .mu.M gene specific reverse primer or 1 .mu.L Oligo(dT).sub.12-18 @ 100 pmoles/.mu.L Total volume 10.5 .mu.L (with RNase-free sterile H.sub.2O)

[0469]Denatured RNA and primer for 10 min at 65.degree. C.

[0470]Immediately cooled on ice.

[0471]Added respective reagents separately to each tube in the following order (no cocktail):

TABLE-US-00045 4 .mu.L 5 x Expand reverse transcriptase buffer (first-strand) (1.times.) 2 .mu.L 100 mM DTT (10 mM) 2 .mu.L 10 mM dNTP Mix (dATP + dCTP + dGTP + dTTP, Roche cat#1581295; 1 mM) 0.5 .mu.L RNase Inhibitor (Roche, cat#799017, 40 U/.mu.L; 20U) 1 .mu.L Expand Reverse Transcriptase (Roche cat#11 785 834 001; 50 U/.mu.L; 50U) Total volume 20 .mu.L(with RNase-free sterile H.sub.2O)

[0472]Mixed and pulse spun.

[0473]Incubated at 43.degree. C. for 45-60 min.

[0474]Quenched on ice.

[0475]Used immediately.

First Round PCR Reaction.

TABLE-US-00046 [0476]5 .mu.L cDNA 1 .mu.L 10 mM dNTP Mix (dATP + dCTP + dGTP + dTTP, Roche cat#1581295; 200 .mu.M) 0.3 .mu.L 25 .mu.M Forward primer (150 nM) 0.3 .mu.L 25 .mu.M Reverse primer (150 nM) 5 .mu.L 10x PCR reaction buffer with MgCl.sub.2 (Roche cat#1 647 679; 1.times.) 1 .mu.L Taq DNA Polymerase (Roche cat#1 647 679; 1 U/.mu.L; 1U) Total volume 50 .mu.L (with sH.sub.2O)

First Round PCR Amplification.

TABLE-US-00047 [0477] 95.degree. C. 2:00 1 cycle 95.degree. C. 0:30 58.degree. C. 0:30 {close oversize brace} 30 cycles 72.degree. C. 2:30 72.degree. C. 7:00 1 cycle

Northern Analysis of RNA

[0478]4 pg pMC6 (Clone 6) used as template.

[0479]Amplified using pMC1 (Clone 1) forward and reverse primers and standard Taq reaction.

[0480]Extracted bands purified using QIAGEN Gel Purification kit.

[0481]Product quantified to 55 ng/.mu.L.

Formaldehyde Gels

[0482]***All water should be sourced fresh from the still.

10.times. MOPS/EDTA Buffer

(A) 52.3 g MOPS (Free Acid, Mr=209, 500 mM)

[0483]Adjust pH to 7.0 with 10N NaOH.

[0484]Final vol 250 mL.

(B) 1.86 g EDTA (Na salt, Mr=372, 10 mM, or 1 mL 500 mM EDTA in 500 mL)

[0485]Adjust pH to 7.5 with 10 N NaOH.

[0486]Final vol 250 mL

[0487]Add 250 mL MOPS to 250 mL EDTA to obtain correct final concentrations.

[0488]Store in the dark at room temperature.

[0489]The buffer may yellow with age or autoclaving but this will not affect buffering capacity.

Buffer A

[0490]300 .mu.L 10.times.MOPS/EDTA Buffer

Final vol 1 mL.

Formaldehyde/Formamide

TABLE-US-00048 [0491] 89 .mu.L AR Formaldehyde (37-40%) 250 .mu.L Formamide (TOXIC. Fumehood and Gloves)

Gel Loading Buffer

TABLE-US-00049 [0492] 400 mg Sucrose 320 .mu.L Buffer A Mix to dissolve then add

TABLE-US-00050 5 mg Xylene cyanol 5 mg Bromophenol blue Mix to dissolve. Add

TABLE-US-00051 178 .mu.L AR Formaldehyde (37-40%) (TOXIC. Fumehood and Gloves) 500 .mu.L Formamide (TOXIC. Fumehood and Gloves) Store in 100 .mu.L aliquots at -20.degree. C.

Running Buffer (=1.times.MOPS/EDTA)

TABLE-US-00052 [0493]225 mL 10.times. MOPS/EDTA Buffer Total vol = 2.25 L

Sample Preparation

TABLE-US-00053 [0494]30 .mu.g RNA (as a dry pellet) 5.5 .mu.L Buffer A Resuspend RNA. Add 12 .mu.L Formamide/Formaldehyde (TOXIC. Fumehood and Gloves) Heat to 70.degree. C. (heating block) for 10 min then quench on ice. Add 4.5 .mu.L Gel Loading Buffer Load onto submerged gel.

Pouring Formaldehyde Gel

[0495]Prepare gel tray by wiping out with ethanol and taping both ends with a double layer of masking tape.

TABLE-US-00054 250 200 125 mL Final vol. 2.5 2.0 1.25 g Agarose 25 20 12.5 mL 10x MOPS/EDTA Buffer 180 144 90 mL H.sub.2O For today's work 2 gels 150 .times. 100 mm prepared with 30-tooth combs in each.

[0496]Mix in a 500 mL flask and dissolve in microwave. Stir while cooling.

[0497]All of following steps should be done in the fumehood:

TABLE-US-00055 Add 45 mL 36 mL 22.5 mL AR Formaldehyde (37-40%)

[0498]Mix and pour into prepared gel tray, with comb in place.

[0499]Allow to set for 30-45 min.

[0500]Cover with Running Buffer, load and run initially at 50V for 15 min to get samples into gel, then turn voltage down to 12V and run overnight.

Northern Blot

20.times.SSC

TABLE-US-00056 [0501]175.3 g AR NaCl (=3M) 88.2 g AR Sodium citrate (=0.3M) Adjust pH to 7.0

Total Volume 1 L

[0502]This Northern Blot method uses the flow of buffer DOWN through a gel then a nylon membrane to transfer denatured RNA from the gel onto the membrane. Based on the design of the Schleicher & Schuell TurboBlotter. [0503]1. Two 3 cm stacks of interfolded paper hand towels (Hygenex Royale, 245.times.270 mm, cat#2170360) were placed side-by-side in a plastic tray [0504]2. Two sheet of 3 mM paper, cut to 220.times.160 mm were placed on top, followed by one sheet pre-wetted in 10.times.SSC. [0505]3. The nylon membrane (Hybond-XL (Amersham; cat no: RPN303S) was cut to 220.times.160 mm, pre-wetted with dH.sub.2O, rinsed for 1 min in 10.times.SSC, and finally placed onto the stack. [0506]4. The gel was removed from the gel plate and washed for 20 min in 10.times.SSC. [0507]5. The washed gel was then placed onto the membrane ensuring that no bubbles were trapped between the gel and the membrane. Note care was taken to ensure that the gel was positioned correctly as transfer may be initiated as soon as the gel comes into contact with the membrane. [0508]6. Three sheets of pre-wetted 3 mM paper, cut to 230.times.170 mm, were layered onto the stack. Again ensuring that no bubbles were trapped between the layers. [0509]7. Finally the pre-wetted 3 mM wick, cut to .about.800.times.180 mm, was placed across the stack, with each end folded over and submerged in 100 mL 20.times.SSC, which was in containers at the side of the blot/stack. [0510]NOTE [0511]1. The wick was kept flat at all times (i.e. the containers were long enough so that the wick did not have to be crammed in). [0512]2. The sides of the containers were only 1-2 cm high so that the capillary action could easily draw the 20.times.SSC up and out of the reservoirs.

Next Day

[0512] [0513]1 The blot was carefully taken apart down to the gel. A soft leaded pencil was pushed through the wells, and used to mark the position of each well on the membrane. [0514]2. The RNA crosslinked to the membrane using a [0515]3. The membrane was then placed between two sheets of dry 3 mM paper and allowed to dry. [0516]4. Finally the membrane was wrapped in Gladwrap and stored at 4.degree. C. overnight.

Labelling the Probes

[0517]RadPrime DNA Labeling System (Invitrogen, Cat. No.: 18428-011)

TABLE-US-00057 1. Denature 25 ng DNA dissolved in 19 .mu.L of sterile distilled water or TE in a microcentrifuge tube by heating for 5 min in a boiling water bath; then immediately cool on ice 2. Perform the following additions on ice: 1 .mu.L 500 .mu.M dATP 1 .mu.L 500 .mu.M dGTP 1 .mu.L 500 .mu.M dTTP 20 .mu.L 2.5X Random Primers Solution 5 .mu.L [.alpha.-32P]dCTP (3000 Ci/mmol. 10 mCi/mL, approximately 50 .mu.Ci) To 49 .mu.L with dH.sub.2O 3. Pulse spin 4. Mix briefly, add 1 .mu.L Klenow Fragment 5. Mix gently but thoroughly 6. Pulse spin 7. Incubate at 37.degree. C. for 10 min 8. Add 5 .mu.L Stop Buffer

Purifying the Probe.

[0518]ProbeQuant G-50 Micro Columns, Amersham Biosciences, cat#27-5335-01. [0519]1. Loosen the lid of the column and snap off the seal at the bottom. [0520]2. Place the column into a 1.5 mL microcentrifuge tube. [0521]3. Spin at 735.times.g for 1 min to remove the liquid. [0522]4. Place the column into a fresh 1.5 mL microcentrifuge tube. [0523]5. Layer the labelled probe onto the column. [0524]6. Spin at 735.times.g for 2 min (unincorporated nucleotides, dyes, and salts will remain on the column). [0525]7. The purified labelled probe will collect in the microfuge tube. [0526]8. Denature the labelled DNA by heating to 95-100.degree. C. for 5 min and snap-cool on ice. [0527]9. Pulse spin. [0528]10. Immediately add into Pre/Hybridisation Solution in tubes (do not place directly onto blot).

[0529]Probing Blots

20.times.SSC

TABLE-US-00058 [0530]175.3 g AR NaCl (=3M) 88.2 g AR Sodium citrate (=0.3M) Adjust pH to 7.0 Total volume 1 L

Pre/Hybridisation Solution.

[0531](from: Church G M & Gilbert W. 1984, Genomic Sequencing, Proc. Natl. Acad. Sci. USA).

TABLE-US-00059 12.5 mL 1M NaHPO.sub.4 Buffer pH 7.2 (250 mM) 20 mL H.sub.2O 100 .mu.L 0.5 M EDTA (1 mM) 17.5 mL 20% SDS (7%) 0.5 g BSA (1%) Final volume ~50 mL.

[0532]Pre-wet blots in 2.times.SSC before placing in hybridisation oven tubes.

[0533]Pre-hybridise in 45 mL Pre/Hybridisation Solution at 65.degree. C. for 2 h.

[0534]Add denatured probe (see above) to the Pre/Hybridisation Solution and hybridise at 65.degree. C. overnight.

Washing Blots

2.times. Wash Buffer

TABLE-US-00060 [0535] 50 mL 20 .times. SSC (2 .times. SSC) 2.5 mL 20% SDS (0.1% SDS) Final volume = 500 mL.

1.times. Wash Buffer.

TABLE-US-00061 [0536] 25 mL 20 .times. SSC (1 .times. SSC) 2.5 mL 20% SDS (0.1% SDS) Final volume = 500 mL.

0.2.times. Wash Buffer.

TABLE-US-00062 [0537] 5 mL 20 .times. SSC (0.2 .times. SSC) 2.5 mL 20% SDS (0.1% SDS) Final volume = 500 mL.

0.1.times. Wash Buffer.

TABLE-US-00063 [0538]2.5 mL 20 .times. SSC (0.1 .times. SSC) 2.5 mL 20% SDS (0.1% SDS) Final volume = 500 mL.

Wash Filters

[0539]2.times. Wash Buffer 2.times.15 min at 65.degree. C. (.about.200 mL per hybridisation tube). [0540]1.times. Wash Buffer 2.times.15 min at 65.degree. C. (.about.200 mL per hybridisation tube). [0541]0.2.times. Wash Buffer 2.times.15 min at 65.degree. C. (.about.200 mL per hybridisation tube). [0542]0.1.times. Wash Buffer 2.times.5 min at 65.degree. C. (.about.200 mL per hybridisation tube).

[0543]Seal membranes in thin plastic bag, check counts using Geiger counter, and expose to X-ray film with intensifying screen at -70.degree. C., overnight (if .about.20 counts per second) or longer depending on signal intensity after washing.

[0544]Blots were exposed for 3 days.

Example 2

Synthetic Sesame Seed Polyoleosin Construction

Background

[0545]We designed a synthetic sesame seed oleosin with tandem repeats for expression in both E. coli as well as plants (e.g., Arabidopsis and Lotus). It should be noted that the oleosin sequence used is for example only. Any oleosin sequence or combinations of oleosins, steroleosins and caoleosins and oleosin linking sequences could be used. The original sesame seed oleosin nucleotide sequence and translated peptide sequence are from a sesame seed oleosin, GenBank clone AF091840 (Tai et al., 2002). The codons were optimised for both E. coli and Arabidopsis expression. Each repeat used randomised degenerate codons to code for the specific amino acid sequence thus ensuring that the repeats will not be rearranged by non rec.sup.- bacteria such as Agrobacterium tumefaciens or Agrobacterium rhizogenes. The construct was designed so that it can be relatively simply subcloned from the original backbone (pUC57) into both pET29a and various plant binary vectors. In order to allow simple restriction digestion and re-ligation to reduce the number of repeats as well as to enable us to paste in future peptides between the repeats we engineered restriction sites between them.

[0546]The design allows various numbers of tandem repeats to be easily transferred into pET29a and to perform simple digestions on the original clone to remove different numbers of inserts then transfer to binary vectors. This included a NcoI site on each end of the sesame oleosin to place it into pET29a which gives the peptide an N-terminal S*Tag and thrombin cleavage site and a C-terminal His.Tag. For transfer to plant binary vectors we designed an attL1 site to the 5' end and an attL2 site to the 3' end, these are compatible for with our GATEWAY plant binary constructs built in house.

[0547]Unique restriction sites (Eco47 .mu.l, DraI, MluNI, SacI, SalI, EcoRI, HindIII, ScaI, HpaI, Alw44I) were also engineered between the repeats to allow future additions of peptides between the repeats. A single oleosin repeat can be generated by XhoI digestion and re-ligation. Similarly, constructs for a dimeric, trimeric and tetrameric oleosin repeats can be generated by digestion and re-ligation with ClaI, BstXI and NdeI respectively. These can then be transferred to chosen binary vectors via the LR reaction. If the intron is not required then this can be removed after transfer to the binary. NotI sites flanked the ORF of the complete clone to allow sub-cloning into pART binary vectors if necessary.

[0548]We have mainly concentrated on constructs using cauliflower mosaic virus 35S promoter (CaMV35S), a well-characterized over-expression promoter. It is expected that polyoleosin expression will only be seen in the seeds of transformed plants where triglyceride will be present (de Boer and Somerville, 2001). We have also created a binary vector containing the Arabidopsis oleosin promoter; this can also be utilised for discreet polyoleosin expression in the seed.

[0549]In addition we created several alternative trimeric oleosin-repeat constructs, In E. coli, we have had success expressing a trimer of direct repeats of the sesame oleosin that was successfully expressed by Dr. Bocky Chi-Chung Peng (Peng et al., 2004). We created two binary vectors (CaMV35S and Oleosin promoters) containing this direct repeat trimer. These constructs have been transformed into Arabidopsis.

Codon Analysis

[0550]We compared the codon usage by both E. coli and Arabidopsis (Table 17). From this we were able to identify codons that were not suitable for use in this construct; these included the following:

TABLE-US-00064 Arg AGG Arg AGA Arg CGG Arg CGA Arg CGC Ile ATA Leu CTA stop TAG

[0551]These codons were removed from the codon Table, the remaining codons were placed in a spread sheet which randomised the possibilities still available for each amino acid. Thus, while the codon usage was randomised the peptide sequence for the sesame seed oleosin was conserved. The randomisation was repeated 6 times, one for each oleosin repeat. An alignment of these sequences showed that the homology dropped to approximately 75% between each repeat and the drop in homology was generally distributed evenly across the whole sequence.

TABLE-US-00065 TABLE 17 Comparison of E. coli and A. thaliana codon usage. ##STR00017## ##STR00018## ##STR00019## ##STR00020## ##STR00021## ##STR00022## ##STR00023## ##STR00024## ##STR00025## ##STR00026## ##STR00027## ##STR00028## ##STR00029## ##STR00030## ##STR00031## ##STR00032##

[0552]Each number represents the proportion that codon is used to code for the respective amino acid. Codons in grey were not used in the polyoleosin construct since they coded for the respective amino acid less than 10% of the time in either organism. Codons in bold and underlined were removed to raise the GC content and to remove cryptic splice sites and mRNA degradation signals (ATTTA).

Selection and Location of Restriction Sites Between Oleosin Repeats

[0553]Restriction sites were inserted as linkers between the repeats. The sites were chosen to allow the subcloning of different combinations of oleosin repeats; they also allowed for the generation of 8 amino acid linkers between each repeat to allow for free rotation etc. Linkers with undesirable codons were not used.

[0554]The multiple cloning sites of both pUC57 and pET29a allowed the design of a sub-cloning strategy using multiple placements of the following restriction sites within the polyoleosin construct.

TABLE-US-00066 Bst XI Cla I Pst I Nco I Nde I Not I Xho I

[0555]The randomised oleosin repeats were checked for these sites and alternative codons were then used to eliminate the sites when discovered.

Unique Restriction Sites

[0556]We also engineered unique Eco47 III, Dra I, Mlu NI, Sac I, Sal I, Sca I, Hpa I, Alw44I sites between different repeats. These have been included to allow future additions of peptides between the repeats.

Not I Sites

[0557]Not I sites flank the ORF of the complete clone. This is to allow sub-cloning into pART binary vectors if necessary.

[0558]A schematic diagram of the construct is shown in FIG. 66.

Optimisation for: Improving Translation Efficiency; Increasing RNA Stability; Correct Splicing.

Tetranucleotide Stop Codon.

[0559]Brown et al., (1990) reported that there was an increasing number of reports where the tri-nucleotide stop codons do not signal the termination of protein synthesis; they found that the signals UAA(A/G) and UGA(A/G) are the preferred stop codons in eukaryotes. Hence we have added an A to the 3' end of the second stop codon (TGA) in our construct.

mRNA Degradation Signal

[0560]Beelman and Parker (1995) reported the degradation signal ATTTA (AUUUA) can destabilize transcripts in plants as well as animals. The proposed construct ORF originally had 7 ATTTA sites. These were predominantly caused by the sequence coding for isoleucine followed by a tyrosine residue. The ATTTA sites were removed by changing the relevant isoleucine codons to ATC. Re-analysis of the splice sites after the removal of the ATTTA sites showed that fewer regions were predicted to be introns (partially determined by the GC content).

pOly T

[0561]The original proposed construct ORF would have had 27 TTTT sites and 12 TTTTT sites.

[0562]To reduce the number of these regions the phenylalanine codon TTT was removed and replaced by TTC; in one case the site was eliminated by moving the engineered DraI site to the 5' end of the Mlu NI site. Combined these changes reduced the number of TTTT sites to 14 and the number of TTTTT sites to 1.

Plant Intron Insertion

[0563]The insertion of a recognised plant intron into an expression construct frequently results in a significantly enhanced expression of the construct in planta; this is termed Intron Mediated Enhancement (Rose 2004 and references therein). The sequence and position of the intron is important in terms of expression enhancement with the highest gains obtained by placing the Arabidopsis thaliana ubiquitin10 (UBQ10) intron within the first 250 bases or so of the 5' end of the transcript (Rose, 2002; 2004 and references therein). Rose and Beliakoff (2000) found that utilising a PstI site was a useful way to insert introns. This was achieved by engineering a PstI site to the 5' end of the intron and by modifying the existing 3' end of the intron to contain a PstI site, from this they were able to add or delete functional introns wherever a PstI site existed in the gene or cDNA.

[0564]Vector NTI identified approximately 4 PstI sites within the proposed polyoleosin construct with the closest to the 5' end occurring approximately 500 bases downstream. All these sites were eliminated using various combinations of degenerate codons and a new PstI site was engineered at position 300 using the degenerate codons. This places the intron in the first oleosin repeat and therefore enables the generation of all truncated versions with the intron (see Sub-Cloning Strategy below). Using the UBQ10 intron sequence (Norris et al., 1993) we engineered the 3' end to include a PstI site; the comparison with the original sequence is shown in FIG. 67.

[0565]The new polyoleosin construct (containing the intron) was then analysed by NetGene2 (Hebsgaard et al., 1996; Brunak et al., 1991, web site address http://www.cbs.dtu.dk/services/NetGene2/) to confirm that the engineered intron would be predicted to be spliced correctly. This analysis revealed that not only would the UBQ10 be spliced out correctly but there were also high confidence cryptic donor and acceptor sites that would likely result in aberrant splicing. The putative cryptic splice sites were either eliminated wherever possible or reduced in confidence by using alternative redundant codons. The analysis was repeated and showed that the only high confidence donor and acceptor sites remaining were flanking the engineered UBQ10 intron (NetGene 2 results of both the polyoleosin prior to cryptic splice site removal and polyoleosin with intron and cryptic splice sites removed are shown below); it was predicted that the splicing would remove only the intron and would leave the construct in frame. The analysis showed that a number of regions did not appear to be coding regions and as such may be susceptible to some aberrant splicing. To further reduce the possibility of cryptic splicing we then modified the GC content of the construct (see GC content below).

GC Content

[0566]Oleosins with optimised and randomised codons; no ATTTA sites or TTT were still found to have relatively low GC content compared to the original sequence. To increase the GC content the additional codons were removed: ATT, AAT, TTA, CTT; this raised the GC content to close to the original content (Table 18).

[0567]The repeats were linked using the previously engineered linking regions. These sequences were modified to remove all but the first Pst I sites in the first oleosin repeat and the removal of an Xho site in the second oleosin repeat. In our construct the ORF has no ATTTA or TTTT sites. Furthermore, when the sequence was re-analysed by NetGene2 the only predicted intron splice site in the ORF was the UBQ10 intron engineered into the PstI site and the % identity of the repeats increased from an average of 74.8% identical to 79.1% identical.

[0568]NetGene2 was used to predict the splicing of the proposed construct. The results indicated that the RNA should only be spliced at the acceptor and donor sites of the UBQ10 intron (Table 19 and FIG. 68).

Conformation of Sequence

[0569]The coding sequence of the complete ORF (after splicing) was then checked against a heptameric repeat of the original oleosin translated sequence and found to be identical over the oleosin coding regions (FIG. 69).

[0570]The sequence and feature map of the proposed construct is shown in FIG. 70 and the vector map is shown in FIG. 71.

Sub-Cloning Strategy.

Plant Intron Removal

[0571]The intron is designed to be removed by Pst I digestion, fragment removal and re-ligation. However, due to the presence of a Pst I site in the multiple cloning site of pUC57 it would be necessary to perform a partial digestion to remove this fragment. It would be preferable to attempt this at least once in order to generate full length clones with and without the intron in the initial cloning vector. Alternatively the full length clones can be transferred to expression vectors prior to Pst I digestion as detailed above.

Transfer to E. coli Expression Vector pET29a and Generation of Different Number of Repeats.

[0572]Transfer the complete clone via partial NcoI digestion then re-ligation into pET29a. The intron can then be removed by Pst I digestion and re-ligation. Full Nco I digestion of the original clone then transfer to pET29a will also yield two trimeric oleosin clones, one will contain the intron. All NcoI digests going into pET29a will have to also be checked for orientation, as this step is not directional. Following intron removal in pET29a a single oleosin repeat can be generated by Xho I digestion and re-ligation. Similarly, constructs for a dimeric, trimeric and tetrameric oleosin repeats can be generated by digestion and re-ligation with Cla I, Bst Xl and Nde I respectively.

Transfer to pRS Series of GATEWAY Adapted Binary Vectors and Generation of Different Number of Repeats.

[0573]A single oleosin repeat can be generated by Xho I digestion and religation. Similarly, constructs for a dimeric, trimeric and tetrameric oleosin repeats can be generated by digestion and re-ligation with Cla I, Bst Xl and Nde I respectively. These can then be transferred to chosen binary vectors via the LR reaction. If the intron is not required then this can be removed after transfer to the binary vector or by partial digestion in pUC57.

TABLE-US-00067 TABLE 18 Comparison of GC content of each synthetic oleosin repeat and the original oleosin sequence. Original Oleosin Repeat Number Construct Design Oleosin 1 2 3 4 5 6 Oleosins with initial selection of optimised 60.9% 54% 54% 53% 57% 56.8% 53.8% and randomised codons; no ATTTA sites or TTT codons Oleosins with initial selection of optimised 60.9% 58.7% 59.1% 59.8% 60.5% 59.5% 57.7% and randomised codons; no ATTTA sites or TTT codons and additionally no ATT, AAT, TTA or CTT codons

TABLE-US-00068 TABLE 19 NetGene2 tabulated output prediction of splicing in polyoleosin after manual removal of cryptic splice sites plus the addition of the UBQ10 intron and enriched GC content. The predicted cryptic splice site at position 97 was ignored since this is in the attL1 site and is not part of the transcribed region. With Intron, optimised codons, enriched GC content, RNA stability modifications Donor splice sites, direct strand 5' exon intron pos 5'->3' phase strand confidence 3' 332 2 + 1.00 GTACCTGCAG{circumflex over ( )}GTAAATTTCT H Acceptor splice sites, direct strand 5' intron exon pos 5'->3' phase strand confidence 3' 97 1 + 0.90 AAAAAAGCAG{circumflex over ( )}GCTCCGCGGC 635 1 + 1.00 TGATCTGCAG{circumflex over ( )}TCATCACAAT H Branch points, direct strand acceptor branch 5' A pos 5'->3' pos 5'->3' strand score 3' 97 52 + -2.41 CAACAAATTGATAAGCAATG 635 617 + -3.71 GATTAATCTGAGTTTTTCTG

Prokaryotic Expression Constructs.

[0574]Three sesame seed oleosin direct repeat constructs were used to generate the prokaryotic expression constructs (FIGS. 66, 72 and 73). One clone provided by Dr Bocky Peng (Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, Taiwan 40227) contained a single oleosin clone using the cDNA nucleotide sequence obtained from the sesame seed oleosin clone as reported by Peng et al., (2004). A second clone generated synthetically by GENEART AG contained 3 identical tandem repeats of the cDNA nucleotide sequence obtained from the sesame seed oleosin clone (FIG. 73); each repeats was linked with a nucleotide sequence encoding glycine-glycine-glycine-glycine-serine-glycine-glycine-glycine-glycine-se- rine (GGGGSGGGGS) (Seq ID No. 22). The third clone was the synthetic sesame seed oleosin hexameric repeat generated by GENEART AG (FIG. 66). Combinations of the GENEART AG synthesised clones including the prokaryotic specific constructs and the plant optimised construct were used to generate prokaryotic expression vectors in the Novagen pET29 backbone containing between 1 to 6 repeats of the oleosin transcript (FIGS. 74-83).

[0575]The first new synthetic oleosin clone was designed around the sesame seed oleosin minus the six C terminal amino acids but a different C terminal linker to the 6.times.His tag. Successful expression of this clone in the pET29a vector would indicate that a specific C terminal linker amino acid sequence is not essential for successful expression. The design of the linker also allows for many different oleosin sequences/repeats to be cloned into the 3' region of the clone, including components of the existing synthetic oleosin sequence with altered codons.

[0576]In the synthetic sesame seed oleosin identical triplicate nucleotide repeat clone (FIGS. 73 and 83), the linker sequence between each unit in the repeat has a repetitive amino acid motif of GGGGSGGGGS, which is designed to allow free movement of each unit in relation to the other units. The C terminal sequence is also be the same as C terminal sequence from the protein expressed by p29Ole, i.e., the single sesame seed oleosin construct. A summary of the constructs and their design is listed in Table 20.

TABLE-US-00069 TABLE 20 Constructs in the pET29 (Novagen) backbone for sesame seed polyoleosin expression in E. coli. Number of sesame seed Construct oleosin Source of name Purpose repeats repeats p29Ole prokaryotic expression 1 original cDNA (FIG. 83) p29Ole2-6xHis prokaryotic expression 2 triplet identical repeats from GENEART AG clone (FIG. 73) p29PS3a prokaryotic expression 3 first 3 randomised codon repeats from GENEART AG (FIG. 70) p29PS3b prokaryotic expression 3 second 3 random repeats from GENEART AG (FIG. 70) p29Ole3+ prokaryotic expression 3 Triplet identical repeats from GENEART AG (FIG. 73) p29Ole4-6xHis prokaryotic expression 4 Original cDNA and triplicate identical repeats from GENEART AG (FIG. 73) p29Ole5-6xHis prokaryotic expression 5 Triplicate identical repeats from GENEART AG (FIG. 73) p29Ole6-6xHis prokaryotic expression 6 randomised codon repeats from GENEART AG (FIG. 70)

Generation of Polyclonal Antibodies to Sesame Seed Oleosin

Culture and Induction of Expression System

[0577]A 50 mL LB broth, supplemented with 50 .mu.g/L kanamycin (Kan50), was inoculated with a loop of pET29 (containing the nucleotide sequence encoding a single sesame seed oleosin with a C-terminal His tag) culture from a plate and incubated 37.degree. C. 200 rpm overnight (16 h). The following day 6 mL aliquots of the overnight culture were used to inoculate 2.times.125 mL LB Kan50 broths in 1 L conical flasks (initial OD600=0.16). The cultures were incubated 37.degree. C. 200 rpm for .about.2 h (OD.sub.600=0.6) and IPTG was added to a final concentration of 0.24 mg/mL (1 mM). The induced cultures were returned to incubate at 37.degree. C. 200 rpm for a further 4 h. The cultures were transferred to 250 mL centrifuge pots and spun at 4000.times.g 4.degree. C. for 10 min (5000 rpm, Sorvall, SS34 rotor).

[0578]The supernatant was discarded and the remaining cells were lysed by adding 10 mL of B PER.RTM. Reagent (Novagen) to the pellet and vortexing/pipetting up and down until the cell suspension was homogeneous. The lysed culture was then incubated with gentle mixing for 20 min. Soluble proteins were separated from insoluble proteins by centrifugation at 12,000.times.g 4.degree. C. for 25 min (13,400 rpm, microfuge). The supernatant was discarded (i.e. retained insoluble proteins in pellet). To increase the purity of the inclusion bodies, 5 mL B PER.RTM. Reagent+200 .mu.g/mL lysozyme was added to the pellet, which was then vortexed/pipetted up and down to resuspend. The mixture was then incubated at RT for 5 min, then spun at 12,000.times.g 4.degree. C. for 25 min (13,400 rpm, microfuge). The supernatant was discarded (i.e. retained insoluble proteins in pellet, pellet very diffuse) and pellet/dissolved inclusion bodies was resuspended in 4 mL Binding Buffer (100 mM NaPO.sub.4, pH8.0, 500 mM NaCl, 6M urea and 10 mM imidazole). To remove debris the mixture was spun at 12,000.times.g 4.degree. C. for 15 min (13,400 rpm, microfuge).

Ni-Agarose Purification and Concentration of His-Tagged Recombinant Protein

[0579]2 mL aliquots of Invitrogen Ni agarose slurry was placed into two empty columns (A and B) and spun in a hand-operated centrifuge to remove storage buffer. To equilibrate the columns 3.times.4 mL Binding Buffer was passed through the columns, spinning in the hand-operated centrifuge between each equilibration. The lysate was added to the column and the Ni agarose was gently resuspended into the lysate. The columns were incubated at RT for 10 min with gentle end-over-end mixing then spun in a hand-operated centrifuge to remove post bind filtrate. To remove non-bound proteins the columns were washed 3.times.4 mL Wash Buffer (100 mM NaPO.sub.4, pH8.0, 500 mM NaCl, 6M urea and 50 mM imidazole), spinning in a hand-operated centrifuge between each wash. Note that the Wash Buffer previously contained 25 mM imidazole the higher concentration (50 mM) was found to increase the purity of the His-tagged target protein in the eluted fractions. Finally, fractions were eluted in the following sequential volumes of Elution Buffer (100 mM NaPO.sub.4, pH8.0, 500 mM NaCl, 6M urea and 250 mM imidazole), with spinning in a hand-operated centrifuge between each fraction: 1 mL (fraction 1), 2 mL (fraction 2), 1 mL (fraction 3), 1 mL overnight (fraction 4).

[0580]200 .mu.L of fraction 3A and 3B was removed and put aside, fractions 1A, 2A, and the remainder of fraction 3A were pooled as were fractions 1B, 2B, and the remainder of fraction 3B giving approximately 2.5 mL each. Each pool was placed into a spin concentrator with a 10 kD molecular weight cut off. The concentrators were spun 3181.times.g 4.degree. C. for 60 min. The concentrate was transferred to a fresh tube and the membrane washed with 2.times.100 uL of the respective retained Fraction 3, the washes were then added to the concentrate.

Whole Gel Elution/Purification of Target Protein

[0581]Whole gel elution was performed using the Bio Rad Mini Whole Gel Eluter as per manufacturers instructions. A denaturing elution buffer was used (250 mM Tris, 125 mM boric acid, 0.1% SDS, check final pH=8.7) and the gel was eluted at 85 mA (constant) for 25 min.

[0582]The whole gel elution technique was used to increase the purity of a sample of Ni.sup.2+ agarose purified recombinant sesame oleosin. Table 21 outlines the loss of recombinant protein that occurred at each stage of the purification process.

TABLE-US-00070 TABLE 21 Protein losses during the whole gel elution procedure. Total Protein Volume Remaining Following . . . (.mu.g) (.mu.L) (%) Ni-agarose column 4106 830 100 Concentration 978 60 24 Whole gel elution 272 3000 7 Concentration 83 70 2

[0583]Following the whole gel elution the gel (FIG. 84) and cellophane (not shown) were Coomassie stained to try to identify where the loss had occurred.

[0584]An intense band of the same molecular weight as the oleosin could be seen both in the gel and on the cellophane. This indicated that the region of the gel containing the oleosin had not been completely over one of the slots in the whole gel eluter, and only an estimated 40% of the target protein was actually eluted from the gel. The presence of oleosin on the cellophane membrane suggested that the oleosin was either precipitating out at high concentrations or the oleosin was binding to the cellophane, which is possible given the hydropathic clusters within the protein.

Ni Agarose Chromatography Affinity Purification

[0585]Following the failure of the whole gel elution another culture was prepared and passed through two Ni2+ agarose affinity columns (A and B) and washed at a high stringency (50 mM imidazole). Eluted fractions were analysed by Coomassie stained SDS PAGE (FIG. 85) and the protein concentration of fractions 1A and 1B was measured using the Bradford's Assay (Table 22).

TABLE-US-00071 TABLE 22 Protein concentration of selected fractions from Ni.sup.2+ agarose purification. Final Final uL in vol. amt. Sample Read 1 Read 2 Average ug rxn ug/uL (uL) (ug) 1A 0.584 0.583 0.584 2.65 1 2.65 400 1060 1B 0.608 0.605 0.608 2.86 1 2.86 400 1146

Raising Antibodies in Rabbits

[0586]The first injection was prepared by mixing equal amount of Freunds Complete Adjuvant and the solution containing 265 .mu.g of the target protein, to a maximum final volume of 0.5 mL. The injection was then administered into multiple sites across the back of the neck and shoulder area of the rabbit. Booster shots containing 77 .mu.g of the target protein were delivered 3 4 weeks after the primary. Then 10-14 days later a test bleed of .about.3 mL was removed for preliminary analysis.

[0587]Bleeds were normally stored overnight at 4.degree. C. The following day this was spun at 1500.times.g 4.degree. C. for 5 min. Clear serum was removed from the top of the clot and initially stored as 200 .mu.L aliquots at 20.degree. C. After thawing, phenol and methiolate was added to the serum (to a final concentration of 0.25% and 0.01% respectively)

Analysis of Rabbit Anti-Sesame Seed Oleosin Antiserum

[0588]Four SDS PAGE gels were prepared and loaded identically with samples containing varying amounts of affinity purified oleosin (first fractions from columns A and B). The gels were run out and three were used for immunoblot analysis and one was silver stained.

[0589]Serum from the test sample was prepared as described above for the rabbit anti-white clover oleosin antisera and used at 1:200 and 1:1000 dilutions (in TBS-Tween) to screen two of the immunoblots. The remaining immunoblot was screened with a 1:200 dilution (in TBS-Tween) of a chicken anti oleosin antibody raised by Professor Jason Tzen (Graduate Institute of Biotechnology, National Chung Hsing University, Taichung, Taiwan 40227). Results from the immunoblot analysis and silver staining are shown in FIG. 86.

Expression and Analysis of 1.times.-6.times. Polyoleosin in E. coli Preparation of E. coli Expression Lines

[0590]100 .mu.L competent E. coli Rosetta cells were transformed with 2.5 .mu.L plasmid DNA. Samples were then incubated on ice for 20 min; heat shocked 42.degree. C. 1 min; cooled rapidly on ice 2 min; and incubated with the addition of 900 .mu.L LB broth at 37.degree. C. 60 min 1400 rpm (Thermomixer). Pelleted cells were spread on LB Kan50 plates and incubated at 37.degree. C. overnight.

Preparation of Artificial Oil Bodies (AOBs)

[0591]The primary methods for investigating the properties of the putative triple sesame polyoleosin protein was to compare with the single sesame recombinant protein in terms of: [0592]AOB size [0593]AOB stability over time and at various temperatures and pH values [0594]Stability of AOBs in the rumen

Day 1

[0595]10 mL LB Kan50 broth toothpick inoculated with original colony from p29Ole3+(8b) and p29Ole, then incubated at 37.degree. C. overnight.

Day 2

[0596]5 mL overnight culture inoculated into a 100 mL LB Kan50 broth (500 mL flask). Incubated 37.degree. C. 150 min. Induced with 400 .mu.L 250 mM IPTG, incubated 37.degree. C. 3 h.

[0597]Each culture was transferred to 2.times.50 mL Falcon tubes and cells pelleted by centrifugation 10 min 4.degree. C. 3200.times.g. Pellet resuspended in 4 mL B Per Reagent (Pierce) and incubated to lyse (RT 20 min, gentle end-over-end mixing).

[0598]Insoluble protein pelleted by centrifugation 20 min 4.degree. C. 3200.times.g. Supernatant discarded and pellets resuspended in 2 mL Oilbody Buffer (total vol.; 50 mM NaPO.sub.4 pH8.0, 50 mM NaCl) and stored at -20.degree. C.

Day 3

[0599]Samples removed from -20.degree. C. and thawed. 2.times.500 .mu.L each prep mixed with 4.5 mL Oilbody Buffer and either 200 .mu.L(A) or 500 .mu.L(B) of purified sesame oil (remaining 1 mL of each prep returned to -20.degree. C.).

[0600]Samples were then sonicated (Sonics & Materials Vibra.about.Cell VC600, 600 W, 20 kHz; 1/8'' tapered micro-tip probe) on ice at Power 4, 80% pulse, 1.times.90 sec (probe heated up at this setting); followed by Power 4, 50% pulse, 2.times.180 sec. After incubation on ice for 90 min the samples were again sonicated on ice at Power 4, 50% pulse, 2.times.180 sec.

[0601]To concentrate the AOBs the samples were spun 10 min 4.degree. C. 3200.times.g and the lower phase decanted off from under upper oilbody phase. Oilbodies were then mixed in 5 mL Oilbody Buffer and completely resuspended by sonication at Power 4, 50% pulse, 1.times.180 sec. The AOBs were then stored at 4.degree. C. until required for subsequent analysis.

[0602]Alternatively, pellets from 20 mL induced cultures of 1.times.6.times. polyoleosin lines were resuspended in 1 mL Oilbody Buffer and sonicated (Sonics & Materials Vibra.about.Cell VC600, 600 W, 20 kHz; 1/8'' tapered micro tip probe) off/on ice at:

TABLE-US-00072 Pulse Time Power 100 20 3 100 20 3 100 20 3 100 20 3

[0603]The mixture was then spun in a microfuge 4.degree. C. 10 min 14,000.times.g (14,500 rpm), the supernatant discarded and 1 mL Oilbody Buffer added to the pellets. 10 .mu.L Purified Sesame Oil added to 240606 samples and 50 .mu.L Purified Sesame Oil added to 210606 samples. Sonicated:

TABLE-US-00073 Pulse Time Power 100 20 3 100 20 3 100 20 3 100 10 5

[0604]Spun in a microfuge 4.degree. C. 15 min 14,000.times.g (14,500 rpm). None of the samples had formed AOBs. Supernatant discarded and 1 mL Oilbody Buffer added to pellets. 50 .mu.L Purified Sesame Oil added to all 240606 and 210606 samples, including those that had already formed AOBs (white layer). Sonicated:

TABLE-US-00074 Pulse Time Power 100 15 5 100 15 5 100 15 5 100 15 5

[0605]Spun in a microfuge 4.degree. C. 15 min 14,000.times.g (14,500 rpm). The supernatant was transferred to a fresh 1.5 mL tube, and the supernatant and AOBs were stored at 4.degree. C. overnight.

[0606]It can be seen by the formation of two layers that (AOB layer=upper), all samples form AOBs including the negative controls (FIG. 87), which consist of induced E. coli Rosetta strain containing the pET22 vector. However, the AOBs formed using non-oleosin E. coli proteins are unstable and rapidly breakdown and coalesce (FIG. 92).

[0607]Alternative methods to prepare artificial oil bodies can also be used including varying the oil/buffer/protein emulsion via different proportions or different oils and buffers. It is also possible to vary the ultrasonic energy required or to dispense with the requirement for ultrasonication via use of other disruptive methods such as vortexing and the use of organic solvents to purify the polyoleosin prior to use.

Analysis of the Purity of Polyoleosins from AOBs

[0608]750 .mu.L Oilbody Buffer added to AOBs, then sonicated:

TABLE-US-00075 Pulse Time Power 100 15 5

[0609]30 .mu.L of each sample was mixed with an equal volume of SDS GLB [@ 2.times.SDS], and the remaining AOBs were stored at 4.degree. C. Protein denatured in boiling water bath for 5 min. Samples loaded onto 12% SDS PAGE [@ 2.times.SDS] gel at 15 .mu.L per lane for the supernatant (S) and 2.5 .mu.L per lane for the AOBs (A). Run at 150V 75 min. After electrophoresis gels were transferred to PVDF membrane for subsequent immunoblot analysis with rabbit anti-oleosin antibodies (FIG. 88). Alternatively samples were loaded onto a 4-15% gradient SDS-PAGE (with no stacking gel) and after electrophoresis gels were stained with SafeStain (Invitrogen) (FIG. 89). Earlier attempts to analyse artificial oil bodies from bacteria by SDS-PAGE showed that varying portions of the 3.times., 4.times., 5.times. and 6.times. samples do not run into the gel, and stop at the stacking/separating gel interface. As it was possible that the polyoleosin proteins with higher numbers of repeats were forming high molecular weight aggregates. This problem is partially alleviated by using SDS/urea denaturing PAGE (Table 23) and visualised using SafeStain (FIG. 90).

TABLE-US-00076 TABLE 23 Recipe for SDS/urea denaturing PAGE. SDS/urea Separating Gel SDS/urea Stacking Gel 2.5 mL 4x Tris-SDS Separating Buffer 5 mL 2x Tris-SDS Stacking Buffer 3 mL 40% Acrylamide 1.25 mL 40% Acrylamide 4.8 g Urea (Mr = 60, 8 M final conc.) 4.8 g Urea (Mr = 60, 8 M final conc.) Made to 10 mL with H.sub.2O Made to 10 mL with H.sub.2O pH adjusted to 8.8 with conc. HCl pH adjusted to 6.8 with 1 M HCl 10 .mu.L TEMED 10 .mu.L TEMED 100 .mu.L 10% APS Washed top of polymerised separating gel with 200 .mu.L aliquots. 100 .mu.L 10% APS * Rinsed wells immediately before loading samples *

AOB Properties

[0610]5 .mu.L aliquots of AOBs were placed on a microscope slide and observed at 1000.times. magnification (FIG. 91). When observed under the microscope the 1.times. oleosin AOBs appeared to be the smallest, and as the number of oleosin repeats increased the average size of the AOBs increased; up to the 3.times. polyoleosin, when AOB size appeared to remain similar for the 3.times., 4.times., 5.times. and 6.times. polyoleosin.

[0611]It is likely that significantly more single oleosin was used to make AOB than any of the multimeric tandem repeat proteins. This would explain the comparatively small size of the 1.times. oleosin AOB size.

AOB Stability Over Time

[0612]A 50 .mu.L aliquot of AOBs was transferred to a 250 .mu.L PCR tube and incubated at 4.degree. C. for 168 h. 5 .mu.L aliquots of the AOBs were then placed on a microscope slide and observed at 1000.times. (FIG. 92). AOB generated from vector control protein extracts showed almost complete coalescence of the oil. After 168 h the size of the AOB in the samples containing recombinant oleosins was inversley related to the number of oleosin repeats. In other words the AOB containing single chain oleosin units were on average larger than those containing 3 linked oleosin units that in turn were on average larger than those containing 6 linked oleosin units (FIG. 92). Thus the long-term stability of the emulsification can be tailored by altering the number of oleosin repeats used to generate the AOB.

AOB Heat Stability

[0613]A 50 .mu.L aliquot of AOBs was transferred to a 250 .mu.L PCR tube and incubated either at 70.degree. C. for 4 h, or at 90.degree. C. for 15 min in a PCR machine. To clearly define the amount of intact AOBs remaining, the tubes were spun 10 min 4.degree. C. 3200.times.g (4000 rpm, Eppendorf 5810R centrifuge, A 4 62 swing out rotor). 5 .mu.L aliquots of the AOBs were then placed on a microscope slide and observed at 1000.times. (FIG. 93).

[0614]Although there did not appear to be much difference in the size of the different AOBs after heat treatment, a large proportion of the AOBs formed with the 1.times. and 2.times. polyoleosins had coalesced (FIG. 93) to form large pools of oil. Those AOBs that were observed from samples formed with the 3.times. polyoleosin were of relatively the same size as before the heat treatment, but had formed a very thick emulsion. Some coalescence was observed in the 4.times. and 5.times. AOBs, but no large pools of oil were observed (FIG. 93). With the 6.times. polyoleosin there was no change in the size of the AOBs, nor was there any evidence of coalescence (FIG. 93). Thus the heat stability of the emulsification can be tailored by altering the number of oleosin repeats used to generate the AOB.

[0615]In addition, thickness of the emulsion layer remaining after heat treatment was correlated with an increase in oleosin repeat number (FIG. 94). Thus the stability of the emulsification at elevated temperatures can be tailored by altering the number of oleosin repeats used to generate the AOB.

Stability of AOB with Different Polyoleosins at pH 3.5, 8.0 and 10.5

[0616]A large number of proteins have been found experimentally to have different optimum pH of maximal stability where pH influences the folding and the net charge of the proteins. We tested for stability of AOBs generated with different polyoleosins at pH 3.5, 8.0 and 10.5.

[0617]Buffers: 50 mM Sodium Phosphate pH 8,100 mM NaC.sub.1-50 [0618]50 mM Glycine-HCl pH 3.5 [0619]50 mm Glycine-NaOH pH 10.5

[0620]AOBs were generated using 1, 2, 3 or 6 polyoleosins; the negative control consisted of AOBs generated using inclusion bodies generated from E. coli containing an empty expression vector. Each preparation was sonicated to evenly suspend them in buffer containing 50 mM sodium phosphate pH 8, 100 mM NaCl. A 25 .mu.l suspension of each polyoleosin-oil body was aliquot into microtubes containing 75 .mu.L of the buffers at different pH. The tubes were incubated at room temperature (.about.22.degree. C.) with every 5 minutes interval of 15 seconds vigorously shaking (.about.1,400 rpm) using a Thermomixer. After approximately 4 hours, samples were taken (.about.4 .mu.L) and dropped on glass slice for microscoping at 1000.times. magnification.

[0621]After 4 hours at room temperature the negative control AOBs were beginning to coalesce at both pH3.5 and 10.5; while no coalescence of the negative control was seen at pH8 the AOBs were no longer spherical (FIG. 95). The AOBs containing 1 oleosin repeat appeared to be unstable at both pH3.5 and 10.5 but were stable at pH8.0. In comparison, AOBs containing 2 or more oleosin repeats were relatively stable at both pH 8.0 and 3.5. At pH 10.5 the AOBs containing 2 or more oleosin repeats were still visible but appeared to be smaller than those in lower pH buffers (FIG. 95). Some precipitation/aggregation of the emulsification was noted in the preparations containing 2 or more oleosin repeats at pH 10.5.

Comparison of Purification of Oleosin by AOB Generation Versus Affinity Purification

[0622]Prokaryotically produced polyoleosins were purified by either AOB generation or Ni.sup.2+ affinity column. These samples were analysed by both SDS-PAGE/immunoblot or Coomassie stain or SafeStain (FIG. 96). This demonstrates that both methods can be used for polyoleosin purification.

Transformation of Arabidopsis thaliana with Polyoleosin Constructs Under the Control of the CaMV35s Construct or the Arabidopsis Oleosin Seed Promoter.

[0623]A range of plant binary vectors containing from 1 to 6 oleosin repeats were created using the synthetic sequences generated by GENEART AG (FIGS. 66, 70, 71 & 72) and two plant binary vectors containing either the CaMV35s promoter or the Arabidopsis oleosin seed promoter (Table 24 and FIGS. 97-116).

TABLE-US-00077 TABLE 24 Summary of constructs generated for expression of polyoleosin in plants. UBQ10 intron Construct Plant Oleosin in first Selectable name promoter Terminator cassette repeat marker pRSh1-PSP1 CaMV35s ocs3' 1 oleosin, yes Spectinomycin & randomised Basta degenerarte codons pRSh1-PSP3 CaMV35s ocs3' 3 oleosins, yes Spectinomycin & randomised Basta degenerate codons pRSh1-PSP4 CaMV35s ocs3' 4 oleosins, yes Spectinomycin & randomised Basta degenerate codons pRSh1-PSP6 CaMV35s ocs3' 6 oleosins, yes Spectinomycin & randomised Basta degenerate codons pRSh3-PSP1 Oleosin ocs3' 1 oleosin, yes Spectinomycin & seed randomised Basta degenerate codons pRSh3-PSP3 Oleosin ocs3' 3 oleosins, yes Spectinomycin & seed randomised Basta degenerate codons pRSh3-PSP4 Oleosin ocs3' 4 oleosins, yes Spectinomycin & seed randomised Basta degenerate codons pRSh3-PSP6 Oleosin ocs3' 6 oleosins, yes Spectinomycin & seed randomised Basta degenerate codons pRSh1-Ole3+ CaMV35s ocs3' 3 oleosins, no Spectinomycin & identical Basta nucleotides codons

Analysis of Agrobacterium Plasmid Preps

[0624]Agrobacterium tumefaciens (strain GV3101) was transformed using the freeze thaw method. 5 .mu.g of plasmid was added to 250 .mu.L of competent GV3101 cells and incubated on ice for 30 min. The cells were then frozen in liquid nitrogen for 1 min and thawed in a 37.degree. C. water bath for 1 min. This process was repeated once then 1 mL LB broth was added to the cell mix. Following incubation at 28.degree. C. for 4-6 h, the cells were pelleted, resuspended in 100 .mu.L LB and plated (20 .mu.L and 50 .mu.L) onto LB Spec.

[0625]Transformed colonies were visualised on LB spec plates after approximately 48 h and single colonies were re streaked on LB spec to ensure the use of single colonies. From these new plates, single colonies were selected and plasmid preps obtained by using 8-10 mL of overnight culture in a modified QIAGEN Mini Prep protocol. Quantification of the preps was by NanoDrop spectrophotometer, and as yields were typically low, the presence of the construct in Agrobacterium was detected by PCR.

Primers

[0626]pRSh1-PSP4:

TABLE-US-00078 (Seq ID No. 23) 35S(3'end)Fwd 5' GAC ACG CTC GAG GAA TTC GGT ACC (Seq ID No. 24) UBQ10IntRev 5' GAT GGT GAT GAC TGC AGA TCA GAA

[0627]Product size=609 bppRSh1-PSP6:

TABLE-US-00079 [0627] UBQ10IntFwd (Seq ID No. 25) 5' CGA TTA ATC TGA GTT TTT CTG ATC TGC AGT CA PolySes3R (Seq ID No. 26) 5' CGA TCA CCG TTC CGG CCA ATG TC

[0628]Product size=889 bp

[0629]The pRSh1-PSP4 primers could be used on any of the 35S promoter polyoleosin constructs.

Cycle

[0630]94.degree. C./2 min

[0631](94.degree. C./30 seq; 63.degree. C./30 sec; 72.degree. C./1 min).times.30

[0632]72.degree. C./7 min

Primers

[0633]pRSh3-PSP4 and pRSh3-PSP6:

TABLE-US-00080 (Seq ID No. 27) OlePro 5' GAC ACG TGA CTT CTC GTC TCC TT (Seq ID No. 28) UBQ10IntRev 5' GAT GGT GAT GAC TGC AGA TCA GAA

[0634]Product size=722 bp

[0635]In theory, these primers will detect any of the plant polyoleosin constructs containing the oleosin promoter. The constructs were thoroughly checked by restriction digestion and sequencing when purified from E. coli. The positive controls were the respective pRSh3-PSP4 and pRSh3-PSP6 plasmid preps from E. coli.

Cycle

[0636]94.degree. C./2 min

[0637](94.degree. C./30 sec; 63.degree. C./30 sec; 72.degree. C./45 sec).times.30

[0638]72.degree. C./7 min

Transformation of Arabidopsis thaliana var Columbia with Polyoleosin Binary Constructs

##STR00033##

[0639]Columbia plants were transformed using the floral dip method. The efficiency of this process can vary depending on a number of variables, including the construct itself, the health and floral development stage of the plant and the strain of Agrobacterium. For some constructs, two variations on the floral dip method were employed in order to try and optimise infiltration effectiveness.

[0640]One method involved dipping the entire plant or pot of plants (Full-dip) into Agrobacterium culture suspended in a solution of 5% (w/v) sucrose and 10 mM magnesium chloride, pH 5.7. Prior to dipping, Silwet L77 (a silicone polyether copolymer) was added to the culture solution to aid infiltration. Plants could be dipped up to three times, at a frequency of no more than once per week. We now have some idea of the efficiency of our full dip method using the polyoleosin constructs, which looks to be about 0.05 0.1%. This indicates that 1 g of T1 seed (approx 50,000 seed) should yield 25 herbicide resistant plants. One batch of 200 dipped plants should yield between 2 g and 5 g of seed.

[0641]The alternative method involved dropping Agrobacterium culture, suspended in the floral dip solution described above, onto individual flowers using a sterile transfer pipette (Floral drop). The rationale here was to avoid the entire plant being covered in Agrobacterium, thus aiding plant recovery. Florets were infiltrated as often as every second day and up to four times in total.

[0642]The seed collected from these transformation events represent T1 seed, which were germinated and sprayed with Basta herbicide in order to select transformed T1 plants. The total number of plants subjected to either of these methods with the different constructs is summarised in Table 25.

TABLE-US-00081 TABLE 25 Summary of Arabidopsis transformations completed with the polyoleosin monomeric, trimeric, tetrameric and hexameric polyoleosin constructs. Approx number of Method of Batch Number Construct Promoter Terminator Resistance plants treated transformation GH 22083 pRSh1-PSP1 CaMV 35S ocs3' Spec/Basta 200 Full-dip GH 22242 pRSh1-PSP1 CaMV 35S ocs3' Spec/Basta 60 Floral drop GH 22243 GH 22082 pRSh1-PSP3 CaMV 35S ocs3' Spec/Basta 200 Full-dip GH 22244 pRSh1-PSP3 CaMV 35S ocs3' Spec/Basta 60 Floral drop GH 22188 GH 22446 pRSh1-PSP4 CaMV 35S ocs3' Spec/Basta 200 Full dip GH 22017 pRSh1-PSP6 CaMV 35S ocs3' Spec/Basta 300 Full dip GH 22150 GH 22171-2 pRSh1-PSP6 CaMV 35S ocs3' Spec/Basta 60 Floral drop GH 22209-10 GH 22447 pRSh3-PSP4 Arabidopsis ocs3' Spec/Basta 200 Full dip oleosin GH 22286 pRSh3-PSP6 Arabidopsis ocs3' Spec/Basta 300 Full dip GH 22430 oleosin GH 22196 pRSh3-PSP6 Arabidopsis ocs3' Spec/Basta 60 Floral drop oleosin GH 22646 pRSh1-Ole3+ CaMV 35S ocs3' Spec/Basta 200 Full dip GH 22485 pRSh3-Ole3+ Arabidopsis ocs3' Spec/Basta 200 Full dip oleosin

PCR Testing of Herbicide Resistant T1 Plants

[0643]T1 seed from batch GH 22017 (Table 25) was collected and 1 g of seed germinated. Spraying with Basta herbicide resulted in approximately 20 herbicide resistant plants. These plants were also tested by PCR on genomic DNA. Genomic DNA was extracted from the rosette leaves of selected plants once they were of a suitable size. Extraction was carried out using the QIAGEN DNeasy mini kit protocol and 100 ng genomic DNA was used as PCR template. Two primer pairs were used to detect different areas of the polyoleosin insertion, thus giving information as to whether any gross rearrangements occurred during integration of the construct into the plant genome.

Plants Transformed with Tandem Repeats of Identical Nucleotide Sesame Seed Oleosin Transcripts.

[0644]The concern with using a construct containing repeating units of exactly the same sequence, as is the case with the Ole3+ constructs, is that non rec.sup.- bacteria such as Agrobacterium may utilise their natural recombination mechanism to rearrange the sequence each time a new generation of bacteria is grown. Most laboratory strains of E. coli have the rec mutation to prevent this phenomenon. The PCR results go some way towards investigating this possibility, by using 2 sets of primers at each end of the repeating unit structure in the constructs. This suggests the constructs are intact after one round of sub-culturing. An additional check is to digest the plasmid preps from Agrobacterium with restriction enzymes and check the banding pattern obtained. The plasmid prep yield from Agrobacterium is typically too low to be able to perform digests, so the prep of clone #1 from each construct was used to transform E. coli TOP10 cells by heatshock. Plasmid preps were prepared by overnight culture of three single colonies and extraction using the Qiagen mini-prep kit. The preps were analysed by three restriction enzymes the correct banding pattern is observed for all the clones tested. This result indicates that the Ole3+ constructs are intact in the Agrobacterium with no rearrangement. In the white clover constructs (discussed above), aberrent RNA species were only found to be expressed in Lotus japonicus roots when the number of identical white clover oleosin repeats was greater than 3. This could be due to rearrangements occurring in the Agrobacterium prior to plant transformation or during the process of stable integration into the plant geneome.

[0645]An additional check of integrity is to sequence through the repeating units of the E. coli preps from TOP10 cells transformed with plasmid obtained from Agrobacterium. We have sequenced through 90% of the repeating units and for the sequence completed, the construct sequence matches with the expected database sequence.

[0646]The possibility of rearrangement is potentially greater as the Agrobacterium integrates its T-DNA into the plant genome. We have no control over this event, so can only check for rearrangement events in the genomic DNA of herbicide resistant plants once they have been identified.

Analysis of Arabidopis thaliana Seeds Expressing Sesame Seed Oleosin.

Protein Expression

[0647]The herbicide resistant Arabidopsis seeds (T1) from the floral dip and full dip plants (T0) were allowed to self and set seed (T2). Seeds were collected from plants as the sliques matured (i.e., turned brown and became dry). Seeds were separated from the sliques and all seeds from 1 plant were pooled. Given the method of transformation the T2 seeds consist of segregating populations. It could be expected that for a single insertion event the T2 seed will demonstrate a 3:1 segregation pattern for a dominant trait (as would be expected for protein expression under the CaMV35s promoter). This would consist of 25% homozygous, 50% hemizygous and 25% wild type (untransformed).

Immunoblot Analysis of Arabidopsis thaliana Oil Bodies Containing Sesame Seed Oleosin.

[0648]T2 seeds from approximately 10 individual transformation events for each construct were analysed for protein expression. Seed lots for analysis were chosen based on the total amount of seed collected per plant.

[0649]Weigh out 25 mg of seed collected from 1 plant; combine with approximately 100 mg of dried, clean sand and 500 .mu.L buffer A (600 mM Sucrose in 10 mM Sodium Phosphate buffer, pH 7.5).

[0650]Grind to a paste using mortar and pestel.

[0651]Recover maximum volume using pipette.

[0652]Rinse mortar and pestel 2.times. with 500 .mu.L buffer A.

[0653]Combine extract and rinse in eppendorf tube, spin at 13 k rpm for 5 minutes.

[0654]Quickly recover the majority of the aqueous layer (bottom layer) using a piptette and transfer to a fresh tube.

[0655]Recover overlying oil layer by piptette after tilting the tube horizontally; transfer to a fresh tube.

[0656]To both fractions (aqueous and oil layer) add buffer A to a final volume of 500 .mu.L; mix by pipetting.

[0657]Mix with equal volumes of loading buffer, vortex, boil for 5 minutes and analyse by SDS-PAGE/immunoblot using rabbit anti-sesame seed oleosin antiserum as the primary antibody (FIG. 117).

[0658]The rabbit anti-sesame seed oleosin antiserum showed no binding with extracts from wild type plants. Immunoreactive protein of the expected size was detected in the plants transformed with the polyoleosin constructs including the monomeric, trimeric and tetrameric constructs (dimeric and tetrameric transformants were not included) (FIG. 117). The SDS-PAGE/immunoblot analysis demonstrates that the constructs can be expressed and translated and that the protein is of the expected molecular weight, it accumulates in the seed and is targeted to the oil bodies in the correct manner. The T2 seed populations screened here contained segregating populations, hence it could be reasonably anticipated that even higher levels of expression would exist in homozygous plants as well perhaps in transgenic plants yet to be analysed. The presences of the immunoreactive band at the molecular weight of the monomeric sesame seed oleosin in all extracts from plants transformed with the polyoleosin trimer and polyoleosin hexamer suggests that either some protein cleavage is occurring or that some of the transcript is only translated as far as the first oleosin repeat before being terminated. The ratio of monomer to either trimer or hexamer is relatively low indicating that the level of accumulation of the monomer is also low.

[0659]SDS-PAGE/Coomassie analysis of the crude protein extracts from seeds of the same samples shows that the level of recombinant protein in the hemizygous transgenic plants is too low to be detected by Coomassie stain in the background of native proteins (FIG. 118).

Properties of Sesame Seed Polyoleosin Expressed in Arabidopsis thaliana Seeds.

Heat Stability

[0660]Oil bodies from two wild type, pRSh1-PSP1, pRSh1-PSP3 and pRSh1-PSP6 Arabidopsis transformants were compared for heat stability. 25 mg of seed from each plant was ground separately in a mortar and pestle containing xx.mu.L oil body extraction buffer (10 mM Sodium Phosphate buffer containing 600 mM sucrose)). This was transferred to a microfuge tube, the mortar and pestle was rinsed a further two times with 500 .mu.L of oil body extraction buffer, combined with the original extract and the volumes were made up to 500 .mu.L with oil body extraction buffer. The tubes were spun at 13 k rpm for 10 minutes and photographed (FIG. 119). Each sample showed a thin layer (containing the oil bodies) floating on the surface of extraction buffer. 400 .mu.L of the oil body extraction buffer was removed using a protein gel loading tip attached to an eppendorf. Small aliquots of oil body extraction buffer were used to resuspend the oil layer and removed to a new 2 ml eppendorf tube. The oil body layers were made up to the same final volume (approximately 500 .mu.L with oil body extraction buffer and resuspended fully by pipetting. 50 .mu.L of the suspension was loaded into PCR tubes and capped; 50 .mu.L was stored at 4.degree. C. The PCR tubes were heated at 90.degree. C. for 2, 4, 24 and 58 hrs. At each time point the tubes were removed from the heating block, spun for 10 minutes at 13 k rpm to separate the suspensions and photographed (FIG. 120). The reduction in oleosin repeat numbers correlates with a decrease in the emulsification layer remaining after 24 hr at 90.degree. C., where the thickest emulsification can be seen from plants expressing the hexameric polyoleosin construct. The reduction in oleosin repeat numbers correlates with a decrease in the emulsification layer remaining after 24 hr at 90.degree. C., where the thickest emulsification can be seen from plants expressing the hexameric polyoleosin construct. At 0 hrs through to 24 hrs at 90.degree. C. the higher the number of oleosin repeats correlates with a thicker emulsification layer. After 58 hrs at 90.degree. C. the oil bodies from the wild type arabidopsis has been reduced to a very thin layer with a small ring of emulsion deposited on the tube above the remaining aqueous phase. In comparison, the ring of emulsion remaining in the transformant samples is much greater (FIG. 120). Thus the stability of the emulsification derived from seed extracts at elevated temperatures can be tailored by altering the number of oleosin repeats used to transform the plant.

REFERENCES

[0661]Beelman C A and Parker R. (1995). Degradation of mRNA ineukaryotes. Cell, 81(2) 179-183. [0662]Bouvier-Nave P, Benveniste P, Oelkers P, Sturley S L, Schaller H. (2000) Expression in yeast and tobacco of plant cDNAs encoding acyl CoA:diacylglycerol acyltransferase. Eur. J. Biochem. 267, 85-96. [0663]Brown C M, Stockwell P A, Trotman C N, Tate W P. (1990). Sequence analysis suggests that tetra-nucleotides signal the termination of protein synthesis in eukaryotes. Nucleic Acids Research. 18(21): 6339-6349. [0664]Brunak, S., Engelbrecht, J., and Knudsen, S. (1991). Prediction of Human mRNA Donor and Acceptor Sites from the DNA Sequence, Journal of Molecular Biology, 220, 49-65) [0665]Christey, M. C. and Braun R. H. 2004. Production of Hairy Root Cultures and Transgenic Plants by Agrobacterium rhizogenes-mediated Transformation p. 47-60. In: L. Pena (ed.), Methods in Molecular Biology, Vol. 286: Transgenic Plants. Humana Press Inc., Totowa, N.J. [0666]Christey, M. C., Sinclair, B. K., Braun, R. H. and Wyke, L. 1997. Regeneration of transgenic vegetable brassicas (Brassica oleracea and B. campestrisl) via Ri-mediated transformation. Plant Cell Reports 16: 587-593. [0667]Dahlqvist A, Stahl U, Lenman M, Banas A, Lee M, Sandager L, Ronne H, Stymne S. (2000) Phospholipid:diacylglycerol acyltransferase: an enzyme that catalyzes the acyl-CoA-independent formation of triacylglycerol in yeast and plants. Proc Natl Acad Sci USA. 97, 6487-6492. [0668]de Boer G-J and Somerville C. (2001). The many changing colours of fatty acid biosynthesis. Proc. Nat. Plant Lipid Cooperative Supplement. Stanford Sierra Summer Camp, Fallen Leaf Lake, Calif.) [0669]Demeyer, D., Doreau, M. 1999. Targets and procedures for altering ruminant meat and milk lipids. Proceedings of the Nutrition Society 58:593-607. [0670]Hebsgaard, S M. Korning, P. G. Tolstrup, N. Engelbrecht, J. Rouze, P. Brunak. S. (1996): Splice site prediction in Arabidopsis thaliana DNA by combining local and global sequence information, Nucleic Acids Research, 24(17)3439-3452. [0671]Lardizabal K D, Mai J T, Wagner N W, Wyrick A, Voelker T, Hawkins D J. (2001) DGAT2 Is a new diacylglycerol acyltransferase gene family. J.B.C. 276, 38862-38869. [0672]Linsmaier, E. M. and Skoog, F. 1965. Organic growth factor requirements of tobacco tissue cultures. Physiol. Plant. 18:100-127. [0673]Murashige, T. and Skoog, F. 1962. A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol. Plant. 15: 473-497. [0674]Norris S R, Meyer S E and Callis J (1993). The intron of Arabidopsis thaliana polyubiquitin genes is conserved in location and is a quantitative determinant of chimeric gene expression. Plant Molecular Biology, 21, 895-906 [0675]Peng C-C, Chen J C F, Shyu D J H, Chen M-J, Tzen J T C. (2004) A system for purification of recombinant proteins in Escherichia coli via artificial oil bodies constituted with their oleosin-fused polypeptides. J. Biotech. 111, 51-57 [0676]Rose A B (2002). Requirements for intron-mediated enhancement of gene expression in Arabidopsis. RNA, 8, 1444-1453 [0677]Rose A B (2004). The effect of intron location on intron-mediated enhancement of gene expression in Arabidopsis. The Plant Journal, 40, 744-751 [0678]Rose A B and Beliakoff J A (2000). Intron-mediated enhancement of gene expression independent of unique intron sequences and splicing. Plant Physiology, 122, 535-542 [0679]Sparrow, P. A. C., Dale, P. J. and Irwin, J. A. 2004. The use of phenotypic markers to identify Brassica oleracea genotypes for routine high throughput Agrobacterium-mediated transformation. Plant Cell Reports 23: 64-70. [0680]Tai, S S K, Chen, M C M, Peng, C C, Tzen J T C. (2002). Gene family of oleosin isoforms and their structural stabilization in sesame seed oil bodies. Biosci. Biotechnol. Biochem. 66(10): 2146-2153. [0681]Tzen J T, Lie G C, Huang A H. (1992). Characterization of the charged components and their topology on the surface of plant seed oil bodies. J Biol. Chem. 267(22):15626-34. [0682]Williams N K, Liepinsh E, Watt S J, Prosselkov P, Matthews J M, Attard P, Beck J L, Dixon N E, Otting G. (2005). Stabilization of native protein fold by intein-mediated covalent cyclization. J. Mol. Biol., 346(4):1095-1108. [0683]Zou J, Wei Y, Jako C, Kumar A, Selvaraj G, Taylor D C. (1999) The Arabidopsis thaliana TAG1 mutant has a mutation in a diacylglycerol acyltransferase gene. Plant J. 19, 645-653.

[0684]Reference to any prior art in the specification is not, and should not be taken as, an acknowledgement or any form of suggestion that this prior art forms part of the common general knowledge in Australia or any other jurisdiction.

[0685]Finally, it is to be understood that various alterations, modifications and/or additions may be made without departing from the spirit of the present invention as outlined herein.

Sequence CWU 1

8314DNAArtificial SequencePrimer sequence 1cacc 4215DNAArtificial SequencePrimer sequence 2tcactcgagg agctc 15312DNAArtificial SequencePrimer sequence 3tctagaggta ct 12412DNAArtificial SequencePrimer sequence 4actagtagta cc 12512DNAArtificial SequencePrimer sequence 5cccgggggta ct 12612DNAArtificial SequencePrimer sequence 6ctgcagagta cc 12712DNAArtificial SequencePrimer sequence 7aagcttggta ct 12812DNAArtificial SequencePrimer sequence 8atcgatagta cc 12915DNAArtificial SequencePrimer sequence 9gtcgacggta cttct 15106DNAArtificial SequencePrimer sequence 10ctcgag 61122DNAArtificial SequencePrimer sequence 11tcagatctcg gtgacgggca gg 221222DNAArtificial SequencePrimer sequence 12atgagccaag aacgacgccc gg 221322DNAArtificial SequencePrimer sequence 13caccatggca caacctcaag tt 221411DNAArtificial SequencePrimer sequence 14gctccaccgc g 111514DNAArtificial SequencePrimer sequence 15tccactagtt ctag 141615DNAArtificial SequencePrimer sequence 16ctagaactag tggat 151713DNAArtificial SequencePrimer sequence 17tcctgcagag tac 131813DNAArtificial SequencePrimer sequence 18gtactctgca gga 131912DNAArtificial SequencePrimer sequence 19atacgatagt ac 122015DNAArtificial SequencePrimer sequence 20ctatcgatac cgtcg 152124DNAArtificial SequencePrimer sequence 21ctcgagtgtt gatctcttag cttc 242210PRTArtificial SequenceLinker sequence 22Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser1 5 102324DNAArtificial SequencePrimer sequence 23gacacgctcg aggaattcgg tacc 242424DNAArtificial SequencePrimer sequence 24gatggtgatg actgcagatc agaa 242530DNAArtificial SequencePrimer sequence 25cgattaatct gagtttttct gatctgcagt 302623DNAArtificial SequencePrimer sequence 26cgatcaccgt tccggccaat gtc 232723DNAArtificial SequencePrimer sequence 27gacacgtgac ttctcgtctc ctt 232824DNAArtificial SequencePrimer sequence 28gatggtgatg actgcagatc agaa 2429628DNATrifolium repens 29caccatggca caacctcaag ttcaagtcca ctcaacaaca acacaccgtc aagaaactgc 60tacctaccca tcaacccaaa acattcgtaa agatgtttac gaaaatgtta actatcccgg 120ccaacgcggt cgttataacg accgctataa tgatagtggt cgttatgatg gtggtattgc 180ctcctttttg tcagagagaa gtcctccagc ctctcaaatc ctcgctaccg ttggaggatt 240tttcataggt ggtactctat ttttattagc tagcatttca tttatcgcca gtcttattgg 300attggcgata atgacaccac tttttatcct ttttagcccg gttttagtcc ctgctgccct 360cactataggg ctagcagtgg ctggaatatt gacagcagat gcttgcgggt tgacggggct 420tatgtcgttg tcgtggaccg tgaaatatgt tagggattta caagcagtag tgcccgaaca 480aatggattcg atgaagggac gtgtcgcgga tgtcgcgagt tatgttggac aaaagactaa 540ggatgttgga caaaaaacta aagaggttgg acaagacata caaacaaaag cacatgaagc 600taagagatca acagtcgacc tcgagtga 62830633DNATrifolium repens 30tctagaggta ctatggcaca acctcaagtt caagtccact caacaacaac acaccgtcaa 60gaaactgcta cctacccatc aacccaaaac attcgtaaag atgtttacga aaatgttaac 120tatcccggcc aacgcggtcg ttataacgac cgctataatg atagtggtcg ttatgatggt 180ggtattgcct cctttttgtc agagagaagt cctccagcct ctcaaatcct cgctaccgtt 240ggaggatttt tcataggtgg tactctattt ttattagcta gcatttcatt tatcgccagt 300cttattggat tggcgataat gacaccactt tttatccttt ttagcccggt tttagtccct 360gctgccctca ctatagggct agcagtggct ggaatattga cagcagatgc ttgcgggttg 420acggggctta tgtcgttgtc gtggaccgtg aaatatgtta gggatttaca agcagtagtg 480cccgaacaaa tggattcgat gaagggacgt gtcgcggatg tcgcgagtta tgttggacaa 540aagactaagg atgttggaca aaaaactaaa gaggttggac aagacataca aacaaaagca 600catgaagcta agagatcaac aggtactact agt 63331613DNATrifolium repens 31cccggggtac tatggcacaa cctcaagttc aagtccactc aacaacaaca caccgtcaag 60aaactgctac ctacccatca acccaaaaca ttcgtaaaga tgtttacgaa aatgttaact 120atcccggcca acgcggtcgt tataacgacc gctataatga tagtggtcgt tatgatggtg 180gtattgcctc ctttttgtca gagagaagtc ctccagcctc tcaaatcctc gctaccgttg 240gaggattttt cataggtggt actctatttt tattagctag catttcattt atcgccagtc 300ttattggatt ggcgataatg acaccacttt ttatcctttt tagcccggtt ttagtccctg 360ctgccctcac tatagggcta gcagtggctg gaatattgac agcagatgct tgcgggttga 420cggggcttat gtcgttgtcg tggaccgtga aatatgttag ggatttacaa gcagtagtgc 480ccgaacaaat ggattcgatg aagggacgtg tcgcggatgt cgcgagttat gttggacaaa 540agactaagga tgttggacaa aaaactaaag aggttggaca agacatacaa acaaaagcac 600aggtactctg cag 61332633DNATrifolium repens 32aagcttggta ctatggcaca acctcaagtt caagtccact caacaacaac acaccgtcaa 60gaaactgcta cctacccatc aacccaaaac attcgtaaag atgtttacga aaatgttaac 120tatcccggcc aacgcggtcg ttataacgac cgctataatg atagtggtcg ttatgatggt 180ggtattgcct cctttttgtc agagagaagt cctccagcct ctcaaatcct cgctaccgtt 240ggaggatttt tcataggtgg tactctattt ttattagcta gcatttcatt tatcgccagt 300cttattggat tggcgataat gacaccactt tttatccttt ttagcccggt tttagtccct 360gctgccctca ctatagggct agcagtggct ggaatattga cagcagatgc ttgcgggttg 420acggggctta tgtcgttgtc gtggaccgtg aaatatgtta gggatttaca agcagtagtg 480cccgaacaaa tggattcgat gaagggacgt gtcgcggatg tcgcgagtta tgttggacaa 540aagactaagg atgttggaca aaaaactaaa gaggttggac aagacataca aacaaaagca 600catgaagcta agagatcaac aggtactatc gat 63333630DNATrifolium repens 33gtcgacggta cttctatggc acaacctcaa gttcaagtcc actcaacaac aacacaccgt 60caagaaactg ctacctaccc atcaacccaa aacattcgta aagatgttta cgaaaatgtt 120aactatcccg gccaacgcgg tcgttataac gaccgctata atgatagtgg tcgttatgat 180ggtggtattg cctccttttt gtcagagaga agtcctccag cctctcaaat cctcgctacc 240gttggaggat ttttcatagg tggtactcta tttttattag ctagcatttc atttatcgcc 300agtcttattg gattggcgat aatgacacca ctttttatcc tttttagccc ggttttagtc 360cctgctgccc tcactatagg gctagcagtg gctggaatat tgacagcaga tgcttgcggg 420ttgacggggc ttatgtcgtt gtcgtggacc gtgaaatatg ttagggattt acaagcagta 480gtgcccgaac aaatggattc gatgaaggga cgtgtcgcgg atgtcgcgag ttatgttgga 540caaaagacta aggatgttgg acaaaaaact aaagaggttg gacaagacat acaaacaaaa 600gcacatgaag ctaagagatc aacactcgag 63034709DNATrifolium repens 34caccatggca caacctcaag ttcaagtcca ctcaacaaca acacaccgtc aagaaactgc 60tacctaccca tcaacccaaa acattcgtaa agatgtttac gaaaatgtta actatcccgg 120ccaacgcggt cgttataacg accgctataa tgatagtggt cgttatgatg gtggtattgc 180ctcctttttg tcagagagaa gtcctccagc ctctcaaatc ctcgctaccg ttggaggatt 240tttcataggt ggtactctat ttttattagc tagcatttca tttatcgcca gtcttattgg 300attggcgata atgacaccac tttttatcct ttttagcccg gttttagtcc ctgctgccct 360cactataggg ctagcagtgg ctggaatatt gacagcagat gcttgcgggt tgacggggct 420tatgtcgttg tcgtggaccg tgaaatatgt tagggattta caagcagtag tgcccgaaca 480aatggattcg atgaagggac gtgtcgcgga tgtcgcgagt tatgttggac aaaagactaa 540ggatgttgga caaaaaacta aagaggttgg acaagacata caaacaaaag cacatgaagc 600taagagatca acagagctcc accgcggtgg cggccgctct agaactagtg gatcccccgg 660gctgcaggaa ttcgatatca agcttatcga taccgtcgac ctcgagtga 709351336DNATrifolium repens 35caccatggca caacctcaag ttcaagtcca ctcaacaaca acacaccgtc aagaaactgc 60tacctaccca tcaacccaaa acattcgtaa agatgtttac gaaaatgtta actatcccgg 120ccaacgcggt cgttataacg accgctataa tgatagtggt cgttatgatg gtggtattgc 180ctcctttttg tcagagagaa gtcctccagc ctctcaaatc ctcgctaccg ttggaggatt 240tttcataggt ggtactctat ttttattagc tagcatttca tttatcgcca gtcttattgg 300attggcgata atgacaccac tttttatcct ttttagcccg gttttagtcc ctgctgccct 360cactataggg ctagcagtgg ctggaatatt gacagcagat gcttgcgggt tgacggggct 420tatgtcgttg tcgtggaccg tgaaatatgt tagggattta caagcagtag tgcccgaaca 480aatggattcg atgaagggac gtgtcgcgga tgtcgcgagt tatgttggac aaaagactaa 540ggatgttgga caaaaaacta aagaggttgg acaagacata caaacaaaag cacatgaagc 600taagagatca acagagctcc accgcggtgg cggccgctct agaggtacta tggcacaacc 660tcaagttcaa gtccactcaa caacaacaca ccgtcaagaa actgctacct acccatcaac 720ccaaaacatt cgtaaagatg tttacgaaaa tgttaactat cccggccaac gcggtcgtta 780taacgaccgc tataatgata gtggtcgtta tgatggtggt attgcctcct ttttgtcaga 840gagaagtcct ccagcctctc aaatcctcgc taccgttgga ggatttttca taggtggtac 900tctattttta ttagctagca tttcatttat cgccagtctt attggattgg cgataatgac 960accacttttt atccttttta gcccggtttt agtccctgct gccctcacta tagggctagc 1020agtggctgga atattgacag cagatgcttg cgggttgacg gggcttatgt cgttgtcgtg 1080gaccgtgaaa tatgttaggg atttacaagc agtagtgccc gaacaaatgg attcgatgaa 1140gggacgtgtc gcggatgtcg cgagttatgt tggacaaaag actaaggatg ttggacaaaa 1200aactaaagag gttggacaag acatacaaac aaaagcacat gaagctaaga gatcaacagg 1260tactactaga actagtggat cccccgggct gcaggaattc gatatcaagc ttatcgatac 1320cgtcgacctc gagtga 1336361958DNATrifolium repens 36caccatggca caacctcaag ttcaagtcca ctcaacaaca acacaccgtc aagaaactgc 60tacctaccca tcaacccaaa acattcgtaa agatgtttac ggaaaatgtt aactatcccg 120gccaacgcgg tcgttataac gaccgctata atgatagtgg tcgttatgat ggtggtattg 180cctccttttt gtcagagaga agtcctccag cctctcaaat cctcgctacc gttggaggat 240ttttcatagg tggtactcta tttttattag ctagcatttc atttatcgcc agtcttattg 300gattggcgat aatgacacca ctttttatcc tttttagccc ggttttagtc cctgctgccc 360tcactatagg gctagcagtg gctggaatat tgacagcaga tgcttgcggg ttgacggggc 420ttatgtcgtt gtcgtggacc gtgaaatatg ttagggattt acaagcagta gtgcccgaac 480aaatggattc gatgaaggga cgtgtcgcgg atgtcgcgag ttatgttgga caaaagacta 540aggatgttgg acaaaaaact aaagaggttg gacaagacat acaaacaaaa gcacatgaag 600ctaagagatc aacagagctc caccgcggtg gcggccgctc tagaggtact atggcacaac 660ctcaagttca agtccactca acaacaacac accgtcaaga aactgctacc tacccatcaa 720cccaaaacat tcgtaaagat gtttacgaaa atgttaacta tcccggccaa cgcggtcgtt 780ataacgaccg ctataatgat agtggtcgtt atgatggtgg tattgcctcc tttttgtcag 840agagaagtcc tccagcctct caaatcctcg ctaccgttgg aggatttttc ataggtggta 900ctctattttt attagctagc atttcattta tcgccagtct tattggattg gcgataatga 960caccactttt tatccttttt agcccggttt tagtccctgc tgccctcact atagggctag 1020cagtggctgg aatattgaca gcagatgctt gcgggttgac ggggcttatg tcgttgtcgt 1080ggaccgtgaa atatgttagg gatttacaag cagtagtgcc cgaacaaatg gattcgatga 1140agggacgtgt cgcggatgtc gcgagttatg ttggacaaaa gactaaggat gttggacaaa 1200aaactaaaga ggttggacaa gacatacaaa caaaagcaca tgaagctaag agatcaacag 1260gtactactag aactagtgga tcccccgggg gtactatggc acaacctcaa gttcaagtcc 1320actcaacaac aacacaccgt caagaaactg ctacctaccc atcaacccaa aacattcgta 1380aagatgttta cgaaaatgtt aactatcccg gccaacgcgg tcgttataac gaccgctata 1440atgatagtgg tcgttatgat ggtggtattg cctccttttt gtcagagaga agtcctccag 1500cctctcaaat cctcgctacc gttggaggat ttttcatagg tggtactcta tttttattag 1560ctagcatttc atttatcgcc agtcttattg gattggcgat aatgacacca ctttttatcc 1620tttttagccc ggttttagtc cctgctgccc tcactatagg gctagcagtg gctggaatat 1680tgacagcaga tgcttgcggg ttgacggggc ttatgtcgtt gtcgtggacc gtgaaatatg 1740ttagggattt acaagcagta gtgcccgaac aaatggattc gatgaaggga cgtgtcgcgg 1800atgtcgcgag ttatgttgga caaaagacta aggatgttgg acaaaaaact aaagaggttg 1860gacaagacat acaaacaaaa gcacatgaag ctaagagatc aacaggtact ctgcaggaat 1920tcgatatcaa gcttatcgat accgtcgacc tcgagtga 195837500DNATrifolium repens 37caacaaayaa cwcaccgtca agaaactgct acctacccat caacccawwa cattcgtaaa 60gatgtttacg aaaatgttaa ctatcccggc caacgcggtc gttataacga ccgctataat 120gatagtggtc gttatgatgg tggtattgcc tcctttttgt cagagagaag tcctccagcc 180accgttggag gatttttcat aggtggtact ctatttttat tagctagcat ttcatttatc 240gccagtctta ttggattggc gataatgaca ccacttttta tctcaaatcc tcgcttcctt 300tttagcccgg ttttagtccc tgctgccctc actatagggc tagcagtggc tggaatattg 360acagcagatg cttgcgggtt gacggggctt atgtcgttgt cgtggaccgt gaaatatgtt 420agggatttac aagcagtagt gcccgaacaa atggattcga tgaagggacg tgtcgcggat 480gtcgcgagtt atgttggaca 50038662DNATrifolium repens 38gatatcaagc ttggtactaw tggcacaacc tcaagttcaa gtccactcaa caacaacaca 60ccgtcaagaa aactgctacc tacccatcaa cccaaaacat tcgtaaagat gtttacgaaa 120aatgtttaac tatcccggcc aacgcggtcg ttataacgac cgctataatg atagtggtcg 180tttatgatgg tggtattgcc tcctttttgt cagagagaag tcctccagcc tctcaaatcc 240tcgctaccgt tggaggattt ttcataggtg gtactctatt tttattagct agcatttcat 300ttatcgccag tcttattgga ttggcgataa tgacaccact ttttatcctt tttagcccgg 360twttagtccc tgctgccctc actatagggc tagcagtggc tggaatattg acagcagatg 420cttgcgggtt gacggggctt atgtcgttgt cgtggaccgt gaaatatgtt agggatttac 480aagcagtagt gcccgaacaa atggattcga tgaagggacg tgtcgcggat gtcgcgagtt 540atgttggaca aaagactaag gatgttggac aaaaaactaa agaggttgga caagacatac 600aaacaaaagc acatgaagct aagagatcaa caggtactat cgataccgtc gacctcgagt 660ga 66239794DNATrifolium repens 39atacaaacaa aagcacatga agctaagaga tcaacaggta ctctgcagga attcgatatc 60aagcttggta ctatggcaca acctcaagtt caagtccact caacaacaac acaccgtcaa 120gaaactgcta cctacccatc aacccaaaac attcgtaaag atgtttacga aaatgttaac 180tatcccggcc aacgcggtcg ttataacgac cgctataatg atagtggtcg ttatgatggt 240ggtattgcct cctttttgtc agagagaagt cctccagcct ctcaaatcct cgctaccgtt 300ggaggatttt tcataggtgg tactctattt ttattagcta gcatttcatt tatcgccagt 360cttattggat tggcgataat gacaccactt tttatccttt ttagcccggt tttagtccct 420gctgccctca ctatagggct agcagtggct ggaatattga cagcagatgc ttgcgggttg 480acggggctta tgtcgttgtc gtggaccgtg aaatatgtta gggatttaca agcagtagtg 540cccgaacaaa tggattcgat gaagggacgt gtcgcggatg tcgcgagtta tgttggacaa 600aagactaagg atgttggaca aaaaactaaa gaggttggac aagacataca aacaaaagca 660catgaagcta agagatcaac aggtactatc gataccgtcg acctcgagtg aaagggtggg 720cgcgccgacc cagctttctt gtacaaagtt ggcattataa gaaagcattg cttatcaatt 780tgttgcaacg aaca 79440609DNATrifolium repens 40atggcacaac ctcaagttca agtccactca acaacaacac accgtcaaga aactgctacc 60tacccatcaa cccaaaacat tcgtaaagat gtttacgaaa atgttaacta tcccggccaa 120cgcggtcgtt ataacgaccg ctataatgat agtggtcgtt atgatggtgg tattgcctcc 180tttttgtcag agagaagtcc tccagcctct caaatcctcg ctaccgttgg aggatttttc 240ataggtggta ctctattttt attagctagc atttcattta tcgccagtct tattggattg 300gcgataatga caccactttt tatccttttt agcccggttt tagtccctgc tgccctcact 360atagggctag cagtggctgg aatattgaca gcagatgctt gcgggttgac ggggcttatg 420tcgttgtcgt ggaccgtgaa atatgttagg gatttacaag cagtagtgcc cgaacaaatg 480gattcgatga agggacgtgt cgcggatgtc gcgagttatg ttggacaaaa gactaaggat 540gttggacaaa aaactaaaga ggttggacaa gacatacaaa caaaagcaca tgaagctaag 600agatcaaca 60941609DNATrifolium repens 41atggcacaac ctcaagttca agtccactca acaacaacac accgtcaaga aactgctacc 60tacccatcaa cccaaaacat tcgtaaagat gtttacgaaa atgttaacta tcccggccaa 120cgcggtcgtt ataacgaccg ctataatgat agtggtcgtt atgatggtgg tattgcctcc 180tttttgtcag agagaagtcc tccagcctct caaatcctcg ctaccgttgg aggatttttc 240ataggtggta ctctattttt attagctagc atttcattta tcgccagtct tattggattg 300gcgataatga caccactttt tatccttttt agcccggttt tagtccctgc tgccctcact 360atagggctag cagtggctgg aatattgaca gcagatgctt gcgggttgac ggggcttatg 420tcgttgtcgt ggaccgtgaa atatgttagg gatttacaag cagtagtgcc cgaacaaatg 480gattcgatga agggacgtgt cgcggatgtc gcgagttatg ttggacaaaa gactaaggat 540gttggacaaa aaactaaaga ggttggacaa gacatacaaa caaaagcaca tgaagctaag 600agatcaaca 60942869DNATrifolium repens 42agatcaacag gtactatcga taccgtcgac ctcgacggta cttctatggc acaacctcaa 60gttcaagtcc actcaacaac aacacaccgt caagaaactg ctacctaccc atcaacccaa 120aacattcgta aagatgttta cgaaaatgtt aactatcccg gccaacgcgg tcgttataac 180gaccgctata atgatagtgg tcgttatgat ggtggtattg cctccttttt gtcagagaga 240agtcctccag cctctcaaat cctcgctacc gttggaggat ttttcatagg tggtactcta 300tttttattag ctagcatttc atttatcgcc agtcttattg gattggcgat aatgacacca 360ctttttatcc tttttagccc ggttttagtc cctgctgccc tcactatagg gctagcagtg 420gctggaatat tgacagcaga tgcttgcggg ttgacggggc ttatgtcgtt gtcgtggacc 480gtgaaatatg ttagggattt acaagcagta gtgcccgaac aaatggattc gatgaaggga 540cgtgtcgcgg atgtcgcgag ttatgttgga caaaagacta aggatgttgg acaaaaaact 600aaagaggttg gacaagacat acaaacaaaa gcacatgaag ctaagagatc aacactcgag 660tgaaagggtg ggcgcgccga cccagctttc ttgtacaaag ttggcattat aagaaagcat 720tgcttatcaa tttgttgcaa cgaacaggtc actatcagtc aaaataaaat cattatttgc 780catccagctg atatccccta tagtgagtcg tattacatgg tcatagctgt ttcctggcag 840ctctggcccg tgtctcaaaa tctctgatg 86943818DNATrifolium repens 43gacatacaaa caaaagcaca tgaagctaag agatcaacag gtactatcga taccgtcgac 60ctcgacggta cttctatggc acaacctcaa gttcaagtcc actcaacaac aacacaccgt 120caagaaactg ctacctaccc atcaacccaa aacattcgta

aagatgttta cgaaaatgtt 180aactatcccg gccaacgcgg tcgttataac gaccgctata atgatagtgg tcgttatgat 240ggtggtattg cctccttttt gtcagagaga agtcctccag cctctcaaat cctcgctacc 300gttggaggat ttttcatagg tggtactcta tttttattag ctagcatttc atttatcgcc 360agtcttattg gattggcgat aatgacacca ctttttatcc tttttagccc ggttttagtc 420cctgctgccc tcactatagg gctagcagtg gctggaatat tgacagcaga tgcttgcggg 480ttgacggggc ttatgtcgtt gtcgtggacc gtgaaatatg ttagggattt acaagcagta 540gtgcccgaac aaatggattc gatgaaggga cgtgtcgcgg atgtcgcgag ttatgttgga 600caaaagacta aggatgttgg acaaaaaact aaagaggttg gacaagacat acaaacaaaa 660gcacatgaag ctaagagatc aacactcgag tgaaagggtg ggcgcgccga cccagctttc 720ttgtacaaag ttgscattat aagaaagcat tgcttatcaa tttgtkgcaa cgaacaggtc 780actatcagtc aaaataaaat ckattatttg ctcgattg 81844304DNAArabidopsis thaliana 44gtaaatttct gtgttcctta ttctctcaaa atcttcgatt ttgttttcgt tcgatcccaa 60tttcgtatat gttctttggt ttagattctg ttaatcttag atcgaagacg attttctggg 120tttgatcgtt agatatcatc ttaattctcg attagggttt catagatatc atccgatttg 180ttcaaataat ttgagttttg tcgaataatt actcttcgat ttgtgatttc tatctagatc 240tggtgttagt ttctagtttg tgcgatcgaa tttgtcgatt aatctgagtt tttctgatta 300acag 30445304DNAArabidopsis thaliana 45gtaaatttct gtgttcctta ttctctcaaa atcttcgatt ttgttttcgt tcgatcccaa 60tttcgtatat gttctttggt ttagattctg ttaatcttag atcgaagacg attttctggg 120tttgatcgtt agatatcatc ttaattctcg attagggttt catagatatc atccgatttg 180ttcaaataat ttgagttttg tcgaataatt actcttcgat ttgtgatttc tatctagatc 240tggtgttagt ttctagtttg tgcgatcgaa tttgtcgatt aatctgagtt tttctgatct 300gcag 30446301DNAArabidopsis thaliana 46gtaaatttct gtgttcctta ttctctcaaa atcttcgatt ttgttttcgt tcgatcccaa 60tttcgtatat gttctttggt ttagattctg ttaatcttag atcgaagacg attttctggg 120tttgatcgtt agatatcatc ttaattctcg attagggttt catagatatc atccgatttg 180ttcaaataat ttgagttttg tcgaataatt actcttcgat ttgtgatttc tatctagatc 240tggtgttagt ttctagtttg tgcgatcgaa tttgtcgatt aatctgagtt tttctgatca 300g 30147870PRTSesamum indicum 47Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His145 150 155 160Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala 165 170 175Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala 180 185 190Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe 195 200 205Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala 210 215 220Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu225 230 235 240Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp 245 250 255Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met 260 265 270Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln 275 280 285Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro 290 295 300His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr305 310 315 320Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 325 330 335Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 340 345 350Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 355 360 365Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val 370 375 380Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala385 390 395 400Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 405 410 415Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 420 425 430Gln Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala 435 440 445Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala 450 455 460Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr465 470 475 480Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val 485 490 495Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu 500 505 510Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser 515 520 525Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly 530 535 540Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg545 550 555 560Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly 565 570 575Ser Gln Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 580 585 590Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala 595 600 605Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 610 615 620Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu625 630 635 640Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu 645 650 655Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 660 665 670Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro 675 680 685Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 690 695 700Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala705 710 715 720Gly Ser Gln Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr 725 730 735Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys 740 745 750Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 755 760 765Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 770 775 780Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe785 790 795 800Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala 805 810 815Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro 820 825 830Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 835 840 845Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 850 855 860Ala Gly Ser Gln Thr Ser865 87048839PRTSesamum indicum 48Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Phe Lys Trp Pro 290 295 300Ser Ala Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ser Ser Ser Glu Leu Pro Trp Val Asp 370 375 380Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu385 390 395 400Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 405 410 415Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 420 425 430Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 435 440 445Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly 450 455 460Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser465 470 475 480Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 485 490 495Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 500 505 510Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 515 520 525Ser His Met Glu Phe Lys Leu Ser Thr Met Ala Glu His Tyr Gly Gln 530 535 540Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln545 550 555 560Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 565 570 575Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 580 585 590Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 595 600 605Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe 610 615 620Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr625 630 635 640Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 645 650 655Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 660 665 670Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn 675 680 685Val His Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro 690 695 700His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr705 710 715 720Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 725 730 735Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 740 745 750Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 755 760 765Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val 770 775 780Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala785 790 795 800Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 805 810 815Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 820 825 830Gln Thr Ser Pro Trp Leu Glu 83549869PRTSesamum indicum 49Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His145 150 155 160Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala 165 170 175Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala 180 185 190Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe 195 200 205Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala 210 215 220Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu225 230 235 240Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp 245 250 255Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met 260 265 270Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln 275 280 285Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro 290 295 300His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr305 310 315 320Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 325 330 335Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 340 345 350Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 355 360 365Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val 370 375 380Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala385 390 395 400Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 405 410 415Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 420 425 430Gln Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala 435 440 445Pro His Leu Gln Leu Gln Pro

Arg Ala Gln Arg Val Val Lys Ala Ala 450 455 460Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr465 470 475 480Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val 485 490 495Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu 500 505 510Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser 515 520 525Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly 530 535 540Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg545 550 555 560Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly 565 570 575Ser Gln Thr Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 580 585 590Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala 595 600 605Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 610 615 620Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu625 630 635 640Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu 645 650 655Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 660 665 670Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro 675 680 685Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 690 695 700Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala705 710 715 720Gly Ser Gln Thr Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 725 730 735Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala 740 745 750Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 755 760 765Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu 770 775 780Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu785 790 795 800Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 805 810 815Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro 820 825 830Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 835 840 845Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala 850 855 860Gly Ser Gln Thr Ser865503289DNAArtificial SequenceSynthetic sequence 50aataatgatt ttattttgac tgatagtgac ctgttcgttg caacaaattg atgagcaatg 60cttttttata atgccaactt tgtacaaaaa agcaggctcc gcggccgctt gctccgttaa 120aaaaaaccat ggcagagcac tacgggcagc agcaacaaac acgtgccccc cacttgcaac 180tgcaaccgcg tgctcagcgt gttgtaaagg cagcgaccgc ggttactgcc ggaggtagcc 240tgttggtgtt atccgggttg accctggctg gaacggtcat tgcgctgaca atcgccacac 300ctctcctggt gatcttctcg cctgtactgg tccctgcagg taaatttctg tgttccttat 360tctctcaaaa tcttcgattt tgttttcgtt cgatcccaat ttcgtatatg ttctttggtt 420tagattctgt taatcttaga tcgaagacga ttttctgggt ttgatcgtta gatatcatct 480taattctcga ttagggtttc atagatatca tccgatttgt tcaaataatt tgagttttgt 540cgaataatta ctcttcgatt tgtgatttct atctagatct ggtgttagtt tctagtttgt 600gcgatcgaat ttgtcgatta atctgagttt ttctgatctg cagtcatcac catcttcctg 660ttgggagcgg gttttctggc aagcggggga tttggtgttg ccgctctgtc tgtgctgtcc 720tggatctacc gttacctgac ggggaaacat ccacccggag cggatcagtt ggagtcggcc 780aagacaaagt tggcgagcaa ggcccgtgaa atgaaggacc gtgccgagca gttcagtcag 840caaccggtag cagggtctca gaccagcatc gatccatcct cctggctcga gatggcggaa 900cactacgggc aacaacagca gactcgtgct ccccacctgc aattacaacc ccgtgcccaa 960cgtgttgtga aagcggcaac agcagtaacg gcagggggaa gtttgctggt cttatcgggg 1020ttgaccttag cgggaaccgt gattgccctg acaattgcga ctccgctgct ggttatcttc 1080agccccgtat tggttccggc cgtgatcacg atttttttgc tgggggcagg atttttagcc 1140agcggaggat ttggggtcgc agcgttgtct gtgctgagtt ggatctatcg ttatttgacc 1200gggaagcacc cacctggagc agaccagctg gagagcgcga aaacgaagct ggcatcgaag 1260gcgcgtgaaa tgaaggatcg tgctgaacaa ttctcccagc agcctgttgc cggttctcag 1320accagccata tgtttaaatg gccaagcgct atggccgagc attatgggca gcaacagcaa 1380acccgtgccc cgcatctgca attgcaacct cgtgcccagc gtgtcgttaa ggcggctact 1440gcggtaacag cgggagggag cttactggta ttaagcgggc tgacattggc cggaacggtg 1500atcgccttaa caatcgcgac acccttgctg gtcatcttca gtccggttct ggtgcccgcg 1560gtgattacga ttttcctgct gggagccggt ttcttagcat cggggggttt tggggtagca 1620gccttgagtg tcctgtcgtg gatctatcgt tacttaactg gaaaacaccc gccaggagct 1680gaccagttgg agtctgcaaa aactaagctg gcgtccaaag cccgtgaaat gaaggatcgt 1740gctgagcagt ttagccagca gccagttgcg ggaagtcaga cctcttcatc tgagctccca 1800tgggtcgaca tggcggagca ttacggtcaa cagcaacaga cccgtgctcc gcacttacaa 1860ttgcaaccac gtgctcaacg tgtcgtaaaa gccgccacgg cagttactgc ggggggatca 1920ttgctggtgt taagtgggtt gacactggcg gggacagtta ttgcactgac gatcgcgacc 1980cccttgttag tgatcttctc ccccgttctg gttccggcgg tcattacaat ctttctgttg 2040ggtgccggat ttttagcctc tgggggattt ggagtagctg ccctgtcagt gttgagctgg 2100atctaccgtt acttaacagg gaagcaccct cccggggcag atcagttgga aagcgccaag 2160accaagctgg caagtaaagc gcgtgaaatg aaggaccgtg ccgaacaatt ttcgcagcaa 2220ccggttgcgg gatcacagac ctctagtact ccatcctcct ggcatatgat ggccgagcac 2280tatggacaac agcagcagac gcgtgcccct catctgcaac tgcaaccccg tgctcaacgt 2340gtcgttaagg ctgcgacagc agtaaccgct gggggttctc tgttagtgtt gtcagggctg 2400actttggcgg ggacggtaat tgcgttgacc attgccaccc cgctgttagt gattttcagc 2460ccggtactgg tgccagcagt tatcacgatc ttcttgctgg gtgccggatt cttggcaagt 2520ggaggttttg gagttgcggc gctgtcagtt ttatcctgga tctatcgtta tctgacagga 2580aaacatcccc caggtgccga tcagctggag agtgccaaga caaaactggc gtctaaggca 2640cgtgaaatga aggatcgtgc cgaacagttt tctcaacagc ccgtagcggg gtcacagacc 2700tcgatcgatc agcaggttaa cgtgcacatg gccgaacatt acggacagca acaacagacg 2760cgtgctccac acctgcaatt gcaaccgcgt gctcaacgtg ttgtcaaagc ggcgaccgcc 2820gtaacagcag gaggatcact gttagtgctg tcgggtttaa ccttggccgg gaccgtcatt 2880gcattgacta ttgcgacgcc cttactggtg atcttttctc cggtgctggt tcccgccgtt 2940attaccatct tcttgttagg ggcaggattc ctggcatcag ggggattcgg agttgcggcg 3000ttgagtgtct taagttggat ctaccgttat ctgactggaa agcacccgcc tggggccgat 3060caactggagt cagccaaaac gaaattggcg tcaaaagcgc gtgaaatgaa ggaccgtgct 3120gagcagtttt ctcagcagcc tgtggcagga tcccagacat caccatggct cgagtaatga 3180agcggccgca cccagctttc ttgtacaaag ttggcattat aagaaagcat tgcttatcaa 3240tttgttgcaa cgaacaggtc actatcagtc aaaataaaat cattatttg 328951914PRTArtificial SequenceSynthetic sequence 51Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Phe Lys Trp Pro 290 295 300Ser Ala Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 370 375 380Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val385 390 395 400Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala 405 410 415Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 420 425 430Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 435 440 445Gln Thr Ser Ser Ser Glu Leu Pro Trp Val Asp Met Ala Glu His Tyr 450 455 460Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg465 470 475 480Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 485 490 495Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu 500 505 510Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 515 520 525Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 530 535 540Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr545 550 555 560Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 565 570 575Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln 580 585 590Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ser Thr Pro Ser 595 600 605Ser Trp His Met Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 610 615 620Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala625 630 635 640Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 645 650 655Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu 660 665 670Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu 675 680 685Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 690 695 700Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro705 710 715 720Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 725 730 735Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala 740 745 750Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn Val His Met Ala Glu 755 760 765His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln 770 775 780Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly785 790 795 800Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile 805 810 815Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu 820 825 830Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala 835 840 845Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr 850 855 860Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser865 870 875 880Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala 885 890 895Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Pro Trp 900 905 910Leu Glu 523291DNAArtificial SequenceSynthetic sequence 52caaataatga ttttattttg actgatagtg acctgttcgt tgcaacaaat tgatgagcaa 60tgctttttta taatgccaac tttgtacaaa aaagcaggct ccgcggccgc ttgctccgtt 120aaaaaaaacc atggcagagc actacgggca gcagcaacaa acacgtgccc cccacttgca 180actgcaaccg cgtgctcagc gtgttgtaaa ggcagcgacc gcggttactg ccggaggtag 240cctgttggtg ttatccgggt tgaccctggc tggaacggtc attgcgctga caatcgccac 300acctctcctg gtgatcttct cgcctgtact ggtccctgca ggtaaatttc tgtgttcctt 360attctctcaa aatcttcgat tttgttttcg ttcgatccca atttcgtata tgttctttgg 420tttagattct gttaatctta gatcgaagac gattttctgg gtttgatcgt tagatatcat 480cttaattctc gattagggtt tcatagatat catccgattt gttcaaataa tttgagtttt 540gtcgaataat tactcttcga tttgtgattt ctatctagat ctggtgttag tttctagttt 600gtgcgatcga atttgtcgat taatctgagt ttttctgatc tgcagtcatc accatcttcc 660tgttgggagc gggttttctg gcaagcgggg gatttggtgt tgccgctctg tctgtgctgt 720cctggatcta ccgttacctg acggggaaac atccacccgg agcggatcag ttggagtcgg 780ccaagacaaa gttggcgagc aaggcccgtg aaatgaagga ccgtgccgag cagttcagtc 840agcaaccggt agcagggtct cagaccagca tcgatccatc ctcctggctc gagatggcgg 900aacactacgg gcaacaacag cagactcgtg ctccccacct gcaattacaa ccccgtgccc 960aacgtgttgt gaaagcggca acagcagtaa cggcaggggg aagtttgctg gtcttatcgg 1020ggttgacctt agcgggaacc gtgattgccc tgacaattgc gactccgctg ctggttatct 1080tcagccccgt attggttccg gccgtgatca cgattttttt gctgggggca ggatttttag 1140ccagcggagg atttggggtc gcagcgttgt ctgtgctgag ttggatctat cgttatttga 1200ccgggaagca cccacctgga gcagaccagc tggagagcgc gaaaacgaag ctggcatcga 1260aggcgcgtga aatgaaggat cgtgctgaac aattctccca gcagcctgtt gccggttctc 1320agaccagcca tatgtttaaa tggccaagcg ctatggccga gcattatggg cagcaacagc 1380aaacccgtgc cccgcatctg caattgcaac ctcgtgccca gcgtgtcgtt aaggcggcta 1440ctgcggtaac agcgggaggg agcttactgg tattaagcgg gctgacattg gccggaacgg 1500tgatcgcctt aacaatcgcg acacccttgc tggtcatctt cagtccggtt ctggtgcccg 1560cggtgattac gattttcctg ctgggagccg gtttcttagc atcggggggt tttggggtag 1620cagccttgag tgtcctgtcg tggatctatc gttacttaac tggaaaacac ccgccaggag 1680ctgaccagtt ggagtctgca aaaactaagc tggcgtccaa agcccgtgaa atgaaggatc 1740gtgctgagca gtttagccag cagccagttg cgggaagtca gacctcttca tctgagctcc 1800catgggtcga catggcggag cattacggtc aacagcaaca gacccgtgct ccgcacttac 1860aattgcaacc acgtgctcaa cgtgtcgtaa aagccgccac ggcagttact gcggggggat 1920cattgctggt gttaagtggg ttgacactgg cggggacagt tattgcactg acgatcgcga 1980cccccttgtt agtgatcttc tcccccgttc tggttccggc ggtcattaca atctttctgt 2040tgggtgccgg atttttagcc tctgggggat ttggagtagc tgccctgtca gtgttgagct 2100ggatctaccg ttacttaaca gggaagcacc ctcccggggc agatcagttg gaaagcgcca 2160agaccaagct ggcaagtaaa gcgcgtgaaa tgaaggaccg tgccgaacaa ttttcgcagc 2220aaccggttgc gggatcacag acctctagta ctccatcctc ctggcatatg atggccgagc 2280actatggaca acagcagcag acgcgtgccc ctcatctgca actgcaaccc cgtgctcaac 2340gtgtcgttaa ggctgcgaca gcagtaaccg ctgggggttc tctgttagtg ttgtcagggc 2400tgactttggc ggggacggta attgcgttga ccattgccac cccgctgtta gtgattttca 2460gcccggtact ggtgccagca gttatcacga tcttcttgct gggtgccgga ttcttggcaa 2520gtggaggttt tggagttgcg gcgctgtcag ttttatcctg gatctatcgt tatctgacag 2580gaaaacatcc cccaggtgcc gatcagctgg agagtgccaa gacaaaactg gcgtctaagg 2640cacgtgaaat gaaggatcgt gccgaacagt tttctcaaca gcccgtagcg gggtcacaga 2700cctcgatcga tcagcaggtt aacgtgcaca tggccgaaca ttacggacag caacaacaga 2760cgcgtgctcc acacctgcaa ttgcaaccgc gtgctcaacg tgttgtcaaa gcggcgaccg 2820ccgtaacagc aggaggatca ctgttagtgc tgtcgggttt aaccttggcc gggaccgtca 2880ttgcattgac tattgcgacg cccttactgg tgatcttttc tccggtgctg gttcccgccg 2940ttattaccat cttcttgtta ggggcaggat tcctggcatc agggggattc ggagttgcgg 3000cgttgagtgt cttaagttgg atctaccgtt atctgactgg aaagcacccg cctggggccg 3060atcaactgga gtcagccaaa acgaaattgg cgtcaaaagc gcgtgaaatg aaggaccgtg 3120ctgagcagtt ttctcagcag cctgtggcag gatcccagac atcaccatgg ctcgagtaat 3180gaagcggccg cacccagctt tcttgtacaa agttggcatt ataagaaagc attgcttatc 3240aatttgttgc aacgaacagg tcactatcag tcaaaataaa atcattattt g 3291531350DNAArtificial SequenceSynthetic sequence 53ttgctccgtt aaaaaaaacc atggctgagc attatggtca acaacagcag accagggcgc 60ctcacctgca gctgcagccg cgcgcccagc gggtagtgaa ggcggccacc gccgtgacag 120ccggcggctc gcttctcgtc ctctctggcc tcactttagc cggaactgtt attgcgctca

180ccatcgccac tccgctgctt gtgatcttta gccccgttct ggtgccggcg gtcataacca 240ttttcttgct gggtgcgggt tttctggcat ccggaggctt cggcgtggcg gcgctgagtg 300tgctgtcgtg gatttacaga tatctgacag ggaaacaccc gccgggggcg gatcagctgg 360aatcggcaaa gacgaagctg gcgagcaagg cgcgagagat gaaggatagg gcagagcagt 420tctcgcagca gcctgttgga ggcggtggat ccggaggcgg tggtagtatg gctgagcatt 480atggtcaaca acagcagacc agggcgcctc acctgcagct gcagccgcgc gcccagcggg 540tagtgaaggc ggccaccgcc gtgacagccg gcggctcgct tctcgtcctc tctggcctca 600ctttagccgg aactgttatt gcgctcacca tcgccactcc gctgcttgtg atctttagcc 660ccgttctggt gccggcggtc ataaccattt tcttgctggg tgcgggtttt ctggcatccg 720gaggcttcgg cgtggcggcg ctgagtgtgc tgtcgtggat ttacagatat ctgacaggga 780aacacccgcc gggggcggat cagctggaat cggcaaagac gaagctggcg agcaaggcgc 840gagagatgaa ggatagggca gagcagttct cgcagcagcc tgttgggggc ggtggatccg 900gtggaggggg atccatggct gagcattatg gtcaacaaca gcagaccagg gcgcctcacc 960tgcagctgca gccgcgcgcc cagcgggtag tgaaggcggc caccgccgtg acagccggcg 1020gctcgcttct cgtcctctct ggcctcactt tagccggaac tgttattgcg ctcaccatcg 1080ccactccgct gcttgtgatc tttagccccg ttctggtgcc ggcggtcata accattttct 1140tgctgggtgc gggttttctg gcatccggag gcttcggcgt ggcggcgctg agtgtgctgt 1200cgtggattta cagatatctg acagggaaac acccgccggg ggcggatcag ctggaatcgg 1260caaagacgaa gctggcgagc aaggcgcgag agatgaagga tagggcagag cagttctcgc 1320agcagcctgt tccatggctc gagtaatgaa 1350542878DNAArtificial SequenceSynthetic sequence 54gaaggagata tacatatgaa agaaaccgct gctgctaaat tcgaacgcca gcacatggac 60agcccagatc tgggtaccct ggtgccacgc ggttccatgg ctgagcatta tggtcaacaa 120cagcagacca gggcgcctca cctgcagctg cagccgcgcg cccagcgggt agtgaaggcg 180gccaccgccg tgacagccgg cggctcgctt ctcgtcctct ctggcctcac tttagccgga 240actgttattg cgctcaccat cgccactccg ctgcttgtga tctttagccc cgttctggtg 300ccggcggtca taaccatttt cttgctgggt gcgggttttc tggcatccgg aggcttcggc 360gtggcggcgc tgagtgtgct gtcgtggatt tacagatatc tgacagggaa acacccgccg 420ggggcggatc agctggaatc ggcaaagacg aagctggcga gcaaggcgcg agagatgaag 480gatagggcag agcagttctc gcagcagcct gttccatggc tgatatcgga tccgaattcg 540agctccgtcg acaagcttgc ggccgcactc gagatggcgg aacactacgg gcaacaacag 600cagactcgtg ctccccacct gcaattacaa ccccgtgccc aacgtgttgt gaaagcggca 660acagcagtaa cggcaggggg aagtttgctg gtcttatcgg ggttgacctt agcgggaacc 720gtgattgccc tgacaattgc gactccgctg ctggttatct tcagccccgt attggttccg 780gccgtgatca cgattttttt gctgggggca ggatttttag ccagcggagg atttggggtc 840gcagcgttgt ctgtgctgag ttggatctat cgttatttga ccgggaagca cccacctgga 900gcagaccagc tggagagcgc gaaaacgaag ctggcatcga aggcgcgtga aatgaaggat 960cgtgctgaac aattctccca gcagcctgtt gccggttctc agaccagcca tatgtttaaa 1020tggccaagcg ctatggccga gcattatggg cagcaacagc aaacccgtgc cccgcatctg 1080caattgcaac ctcgtgccca gcgtgtcgtt aaggcggcta ctgcggtaac agcgggaggg 1140agcttactgg tattaagcgg gctgacattg gccggaacgg tgatcgcctt aacaatcgcg 1200acacccttgc tggtcatctt cagtccggtt ctggtgcccg cggtgattac gattttcctg 1260ctgggagccg gtttcttagc atcggggggt tttggggtag cagccttgag tgtcctgtcg 1320tggatctatc gttacttaac tggaaaacac ccgccaggag ctgaccagtt ggagtctgca 1380aaaactaagc tggcgtccaa agcccgtgaa atgaaggatc gtgctgagca gtttagccag 1440cagccagttg cgggaagtca gacctcttca tctgagctcc catgggtcga catggcggag 1500cattacggtc aacagcaaca gacccgtgct ccgcacttac aattgcaacc acgtgctcaa 1560cgtgtcgtaa aagccgccac ggcagttact gcggggggat cattgctggt gttaagtggg 1620ttgacactgg cggggacagt tattgcactg acgatcgcga cccccttgtt agtgatcttc 1680tcccccgttc tggttccggc ggtcattaca atctttctgt tgggtgccgg atttttagcc 1740tctgggggat ttggagtagc tgccctgtca gtgttgagct ggatctaccg ttacttaaca 1800gggaagcacc ctcccggggc agatcagttg gaaagcgcca agaccaagct ggcaagtaaa 1860gcgcgtgaaa tgaaggaccg tgccgaacaa ttttcgcagc aaccggttgc gggatcacag 1920acctctagta ctccatcctc ctggcatatg atggccgagc actatggaca acagcagcag 1980acgcgtgccc ctcatctgca actgcaaccc cgtgctcaac gtgtcgttaa ggctgcgaca 2040gcagtaaccg ctgggggttc tctgttagtg ttgtcagggc tgactttggc ggggacggta 2100attgcgttga ccattgccac cccgctgtta gtgattttca gcccggtact ggtgccagca 2160gttatcacga tcttcttgct gggtgccgga ttcttggcaa gtggaggttt tggagttgcg 2220gcgctgtcag ttttatcctg gatctatcgt tatctgacag gaaaacatcc cccaggtgcc 2280gatcagctgg agagtgccaa gacaaaactg gcgtctaagg cacgtgaaat gaaggatcgt 2340gccgaacagt tttctcaaca gcccgtagcg gggtcacaga cctcgatcga tcagcaggtt 2400aacgtgcaca tggccgaaca ttacggacag caacaacaga cgcgtgctcc acacctgcaa 2460ttgcaaccgc gtgctcaacg tgttgtcaaa gcggcgaccg ccgtaacagc aggaggatca 2520ctgttagtgc tgtcgggttt aaccttggcc gggaccgtca ttgcattgac tattgcgacg 2580cccttactgg tgatcttttc tccggtgctg gttcccgccg ttattaccat cttcttgtta 2640ggggcaggat tcctggcatc agggggattc ggagttgcgg cgttgagtgt cttaagttgg 2700atctaccgtt atctgactgg aaagcacccg cctggggccg atcaactgga gtcagccaaa 2760acgaaattgg cgtcaaaagc gcgtgaaatg aaggaccgtg ctgagcagtt ttctcagcag 2820cctgtggcag gatcccagac atcaccatgg ctcgagcacc accaccacca ccactgag 2878551068DNAArtificial SequenceSynthetic sequence 55gaaggagata tacatatgaa agaaaccgct gctgctaaat tcgaacgcca gcacatggac 60agcccagatc tgggtaccct ggtgccacgc ggttccatgg ctgagcatta tggtcaacaa 120cagcagacca gggcgcctca cctgcagctg cagccgcgcg cccagcgggt agtgaaggcg 180gccaccgccg tgacagccgg cggctcgctt ctcgtcctct ctggcctcac tttagccgga 240actgttattg cgctcaccat cgccactccg ctgcttgtga tctttagccc cgttctggtg 300ccggcggtca taaccatttt cttgctgggt gcgggttttc tggcatccgg aggcttcggc 360gtggcggcgc tgagtgtgct gtcgtggatt tacagatatc tgacagggaa acacccgccg 420ggggcggatc agctggaatc ggcaaagacg aagctggcga gcaaggcgcg agagatgaag 480gatagggcag agcagttctc gcagcagcct gttggaggcg gtggatccgg aggcggtggt 540agtatggctg agcattatgg tcaacaacag cagaccaggg cgcctcacct gcagctgcag 600ccgcgcgccc agcgggtagt gaaggcggcc accgccgtga cagccggcgg ctcgcttctc 660gtcctctctg gcctcacttt agccggaact gttattgcgc tcaccatcgc cactccgctg 720cttgtgatct ttagccccgt tctggtgccg gcggtcataa ccattttctt gctgggtgcg 780ggttttctgg catccggagg cttcggcgtg gcggcgctga gtgtgctgtc gtggatttac 840agatatctga cagggaaaca cccgccgggg gcggatcagc tggaatcggc aaagacgaag 900ctggcgagca aggcgcgaga gatgaaggat agggcagagc agttctcgca gcagcctgtt 960gggggcggtg gatccggtgg agggggatcc atggcgatat cggatccgaa ttcgagctcc 1020gtcgacaagc ttgcggccgc actcgagcac caccaccacc accactga 1068561929DNAArtificial SequenceSynthetic sequence 56gaaggagata tacatatgaa agaaaccgct gctgctaaat tcgaacgcca gcacatggac 60agcccagatc tgggtaccct ggtgccacgc ggttccatgg ctgagcatta tggtcaacaa 120cagcagacca gggcgcctca cctgcagctg cagccgcgcg cccagcgggt agtgaaggcg 180gccaccgccg tgacagccgg cggctcgctt ctcgtcctct ctggcctcac tttagccgga 240actgttattg cgctcaccat cgccactccg ctgcttgtga tctttagccc cgttctggtg 300ccggcggtca taaccatttt cttgctgggt gcgggttttc tggcatccgg aggcttcggc 360gtggcggcgc tgagtgtgct gtcgtggatt tacagatatc tgacagggaa acacccgccg 420ggggcggatc agctggaatc ggcaaagacg aagctggcga gcaaggcgcg agagatgaag 480gatagggcag agcagttctc gcagcagcct gttccatggc gatatcggat ccgaattcga 540gctccgtcga caagcttgcg gccgcttgct ccgttaaaaa aaaccatggc tgagcattat 600ggtcaacaac agcagaccag ggcgcctcac ctgcagctgc agccgcgcgc ccagcgggta 660gtgaaggcgg ccaccgccgt gacagccggc ggctcgcttc tcgtcctctc tggcctcact 720ttagccggaa ctgttattgc gctcaccatc gccactccgc tgcttgtgat ctttagcccc 780gttctggtgc cggcggtcat aaccattttc ttgctgggtg cgggttttct ggcatccgga 840ggcttcggcg tggcggcgct gagtgtgctg tcgtggattt acagatatct gacagggaaa 900cacccgccgg gggcggatca gctggaatcg gcaaagacga agctggcgag caaggcgcga 960gagatgaagg atagggcaga gcagttctcg cagcagcctg ttggaggcgg tggatccgga 1020ggcggtggta gtatggctga gcattatggt caacaacagc agaccagggc gcctcacctg 1080cagctgcagc cgcgcgccca gcgggtagtg aaggcggcca ccgccgtgac agccggcggc 1140tcgcttctcg tcctctctgg cctcacttta gccggaactg ttattgcgct caccatcgcc 1200actccgctgc ttgtgatctt tagccccgtt ctggtgccgg cggtcataac cattttcttg 1260ctgggtgcgg gttttctggc atccggaggc ttcggcgtgg cggcgctgag tgtgctgtcg 1320tggatttaca gatatctgac agggaaacac ccgccggggg cggatcagct ggaatcggca 1380aagacgaagc tggcgagcaa ggcgcgagag atgaaggata gggcagagca gttctcgcag 1440cagcctgttg ggggcggtgg atccggtgga gggggatcca tggctgagca ttatggtcaa 1500caacagcaga ccagggcgcc tcacctgcag ctgcagccgc gcgcccagcg ggtagtgaag 1560gcggccaccg ccgtgacagc cggcggctcg cttctcgtcc tctctggcct cactttagcc 1620ggaactgtta ttgcgctcac catcgccact ccgctgcttg tgatctttag ccccgttctg 1680gtgccggcgg tcataaccat tttcttgctg ggtgcgggtt ttctggcatc cggaggcttc 1740ggcgtggcgg cgctgagtgt gctgtcgtgg atttacagat atctgacagg gaaacacccg 1800ccgggggcgg atcagctgga atcggcaaag acgaagctgg cgagcaaggc gcgagagatg 1860aaggataggg cagagcagtt ctcgcagcag cctgttccat ggctcgagca ccaccaccac 1920caccactga 1929572403DNAArtificial SequenceSynthetic sequence 57gaaggagata tacatatgaa agaaaccgct gctgctaaat tcgaacgcca gcacatggac 60agcccagatc tgggtaccct ggtgccacgc ggttccatgg ctgagcatta tggtcaacaa 120cagcagacca gggcgcctca cctgcagctg cagccgcgcg cccagcgggt agtgaaggcg 180gccaccgccg tgacagccgg cggctcgctt ctcgtcctct ctggcctcac tttagccgga 240actgttattg cgctcaccat cgccactccg ctgcttgtga tctttagccc cgttctggtg 300ccggcggtca taaccatttt cttgctgggt gcgggttttc tggcatccgg aggcttcggc 360gtggcggcgc tgagtgtgct gtcgtggatt tacagatatc tgacagggaa acacccgccg 420ggggcggatc agctggaatc ggcaaagacg aagctggcga gcaaggcgcg agagatgaag 480gatagggcag agcagttctc gcagcagcct gttggaggcg gtggatccgg aggcggtggt 540agtatggctg agcattatgg tcaacaacag cagaccaggg cgcctcacct gcagctgcag 600ccgcgcgccc agcgggtagt gaaggcggcc accgccgtga cagccggcgg ctcgcttctc 660gtcctctctg gcctcacttt agccggaact gttattgcgc tcaccatcgc cactccgctg 720cttgtgatct ttagccccgt tctggtgccg gcggtcataa ccattttctt gctgggtgcg 780ggttttctgg catccggagg cttcggcgtg gcggcgctga gtgtgctgtc gtggatttac 840agatatctga cagggaaaca cccgccgggg gcggatcagc tggaatcggc aaagacgaag 900ctggcgagca aggcgcgaga gatgaaggat agggcagagc agttctcgca gcagcctgtt 960gggggcggtg gatccggtgg agggggatcc atgggatatc ggatccgaat tcgagctccg 1020tcgacaagct tgcggccgct tgctccgtta aaaaaaacca tggctgagca ttatggtcaa 1080caacagcaga ccagggcgcc tcacctgcag ctgcagccgc gcgcccagcg ggtagtgaag 1140gcggccaccg ccgtgacagc cggcggctcg cttctcgtcc tctctggcct cactttagcc 1200ggaactgtta ttgcgctcac catcgccact ccgctgcttg tgatctttag ccccgttctg 1260gtgccggcgg tcataaccat tttcttgctg ggtgcgggtt ttctggcatc cggaggcttc 1320ggcgtggcgg cgctgagtgt gctgtcgtgg atttacagat atctgacagg gaaacacccg 1380ccgggggcgg atcagctgga atcggcaaag acgaagctgg cgagcaaggc gcgagagatg 1440aaggataggg cagagcagtt ctcgcagcag cctgttggag gcggtggatc cggaggcggt 1500ggtagtatgg ctgagcatta tggtcaacaa cagcagacca gggcgcctca cctgcagctg 1560cagccgcgcg cccagcgggt agtgaaggcg gccaccgccg tgacagccgg cggctcgctt 1620ctcgtcctct ctggcctcac tttagccgga actgttattg cgctcaccat cgccactccg 1680ctgcttgtga tctttagccc cgttctggtg ccggcggtca taaccatttt cttgctgggt 1740gcgggttttc tggcatccgg aggcttcggc gtggcggcgc tgagtgtgct gtcgtggatt 1800tacagatatc tgacagggaa acacccgccg ggggcggatc agctggaatc ggcaaagacg 1860aagctggcga gcaaggcgcg agagatgaag gatagggcag agcagttctc gcagcagcct 1920gttgggggcg gtggatccgg tggaggggga tccatggctg agcattatgg tcaacaacag 1980cagaccaggg cgcctcacct gcagctgcag ccgcgcgccc agcgggtagt gaaggcggcc 2040accgccgtga cagccggcgg ctcgcttctc gtcctctctg gcctcacttt agccggaact 2100gttattgcgc tcaccatcgc cactccgctg cttgtgatct ttagccccgt tctggtgccg 2160gcggtcataa ccattttctt gctgggtgcg ggttttctgg catccggagg cttcggcgtg 2220gcggcgctga gtgtgctgtc gtggatttac agatatctga cagggaaaca cccgccgggg 2280gcggatcagc tggaatcggc aaagacgaag ctggcgagca aggcgcgaga gatgaaggat 2340agggcagagc agttctcgca gcagcctgtt ccatggctcg agcaccacca ccaccaccac 2400tga 240358953PRTArtificial SequenceSynthetic sequence 58Met Lys Glu Thr Ala Ala Ala Lys Phe Glu Arg Gln His Met Asp Ser1 5 10 15Pro Asp Leu Gly Thr Leu Val Pro Arg Gly Ser Met Ala Glu His Tyr 20 25 30Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg 35 40 45Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 50 55 60Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu65 70 75 80Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 85 90 95Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 100 105 110Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr 115 120 125Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 130 135 140Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln145 150 155 160Phe Ser Gln Gln Pro Val Pro Trp Leu Ile Ser Asp Pro Asn Ser Ser 165 170 175Ser Val Asp Lys Leu Ala Ala Ala Leu Glu Met Ala Glu His Tyr Gly 180 185 190Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala 195 200 205Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu 210 215 220Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr225 230 235 240Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala 245 250 255Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly 260 265 270Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu 275 280 285Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr 290 295 300Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe305 310 315 320Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Phe Lys Trp 325 330 335Pro Ser Ala Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala 340 345 350Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala 355 360 365Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr 370 375 380Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val385 390 395 400Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu 405 410 415Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser 420 425 430Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly 435 440 445Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg 450 455 460Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly465 470 475 480Ser Gln Thr Ser Ser Ser Glu Leu Pro Trp Val Asp Met Ala Glu His 485 490 495Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro 500 505 510Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly 515 520 525Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala 530 535 540Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val545 550 555 560Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser 565 570 575Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg 580 585 590Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala 595 600 605Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu 610 615 620Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ser Thr Pro625 630 635 640Ser Ser Trp His Met Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr 645 650 655Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys 660 665 670Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 675 680 685Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 690 695 700Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe705 710 715 720Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala 725 730 735Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro 740 745 750Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 755 760 765Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 770 775 780Ala Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn Val His Met Ala785 790 795 800Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu 805 810 815Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala 820 825 830Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val 835 840 845Ile Ala Leu Thr

Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val 850 855 860Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu865 870 875 880Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile 885 890 895Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu 900 905 910Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg 915 920 925Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Pro 930 935 940Trp Leu Glu His His His His His His945 95059350PRTArtificial SequenceSynthetic sequence 59Met Lys Glu Thr Ala Ala Ala Lys Phe Glu Arg Gln His Met Asp Ser1 5 10 15Pro Asp Leu Gly Thr Leu Val Pro Arg Gly Ser Met Ala Glu His Tyr 20 25 30Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg 35 40 45Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 50 55 60Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu65 70 75 80Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 85 90 95Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 100 105 110Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr 115 120 125Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 130 135 140Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln145 150 155 160Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 165 170 175Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu 180 185 190Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 195 200 205Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 210 215 220Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser225 230 235 240Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly 245 250 255Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 260 265 270Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 275 280 285Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 290 295 300Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser305 310 315 320Gly Gly Gly Gly Ser Met Ala Ile Ser Asp Pro Asn Ser Ser Ser Val 325 330 335Asp Lys Leu Ala Ala Ala Leu Glu His His His His His His 340 345 35060637PRTArtificial SequenceSynthetic sequence 60Met Lys Glu Thr Ala Ala Ala Lys Phe Glu Arg Gln His Met Asp Ser1 5 10 15Pro Asp Leu Gly Thr Leu Val Pro Arg Gly Ser Met Ala Glu His Tyr 20 25 30Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg 35 40 45Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 50 55 60Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu65 70 75 80Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 85 90 95Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 100 105 110Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr 115 120 125Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 130 135 140Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln145 150 155 160Phe Ser Gln Gln Pro Val Pro Trp Arg Tyr Arg Ile Arg Ile Arg Ala 165 170 175Pro Ser Thr Ser Leu Arg Pro Leu Ala Pro Leu Lys Lys Thr Met Ala 180 185 190Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu 195 200 205Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala 210 215 220Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val225 230 235 240Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val 245 250 255Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu 260 265 270Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile 275 280 285Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu 290 295 300Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg305 310 315 320Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser Gly Gly 325 330 335Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala 340 345 350Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala 355 360 365Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr 370 375 380Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val385 390 395 400Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu 405 410 415Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser 420 425 430Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly 435 440 445Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg 450 455 460Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly465 470 475 480Gly Gly Ser Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln 485 490 495Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg 500 505 510Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val 515 520 525Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala 530 535 540Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile545 550 555 560Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly 565 570 575Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly 580 585 590Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu 595 600 605Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln 610 615 620Gln Pro Val Pro Trp Leu Glu His His His His His His625 630 63561795PRTArtificial SequenceSynthetic sequence 61Met Lys Glu Thr Ala Ala Ala Lys Phe Glu Arg Gln His Met Asp Ser1 5 10 15Pro Asp Leu Gly Thr Leu Val Pro Arg Gly Ser Met Ala Glu His Tyr 20 25 30Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg 35 40 45Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 50 55 60Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu65 70 75 80Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 85 90 95Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 100 105 110Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr 115 120 125Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 130 135 140Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln145 150 155 160Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser 165 170 175Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu 180 185 190Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 195 200 205Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 210 215 220Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser225 230 235 240Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly 245 250 255Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 260 265 270Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 275 280 285Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 290 295 300Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser305 310 315 320Gly Gly Gly Gly Ser Met Gly Tyr Arg Ile Arg Ile Arg Ala Pro Ser 325 330 335Thr Ser Leu Arg Pro Leu Ala Pro Leu Lys Lys Thr Met Ala Glu His 340 345 350Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro 355 360 365Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly 370 375 380Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala385 390 395 400Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val 405 410 415Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser 420 425 430Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg 435 440 445Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala 450 455 460Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu465 470 475 480Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser Gly Gly Gly Gly 485 490 495Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His 500 505 510Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala 515 520 525Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala 530 535 540Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe545 550 555 560Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala 565 570 575Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu 580 585 590Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp 595 600 605Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met 610 615 620Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly625 630 635 640Ser Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln 645 650 655Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val 660 665 670Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser 675 680 685Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro 690 695 700Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile705 710 715 720Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala 725 730 735Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His 740 745 750Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser 755 760 765Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro 770 775 780Val Pro Trp Leu Glu His His His His His His785 790 79562441PRTArtificial SequenceSynthetic sequence 62Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser 130 135 140Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr145 150 155 160Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys 165 170 175Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 180 185 190Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 195 200 205Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe 210 215 220Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala225 230 235 240Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro 245 250 255Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 260 265 270Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 275 280 285Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly 290 295 300Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala305 310 315 320Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu 325 330 335Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr 340 345 350Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala 355 360 365Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly 370 375 380Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu385 390 395 400Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr 405 410 415Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe 420 425 430Ser Gln Gln Pro Val Pro Trp Leu Glu 435 44063149PRTArtificial SequenceSynthetic sequence 63Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys

115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Pro Trp Leu Glu His 130 135 140His His His His His145642227DNAArtificial SequenceSynthetic sequence 64tcgacgaatt aattccaatc ccacaaaaat ctgagcttaa cagcacagtt gctcctctca 60gagcagaatc gggtattcaa caccctcata tcaactacta cgttgtgtat aacggtccac 120atgccggtat atacgatgac tggggttgta caaaggcggc aacaaacggc gttcccggag 180ttgcacacaa gaaatttgcc actattacag aggcaagagc agcagctgac gcgtacacaa 240caagtcagca aacagacagg ttgaacttca tccccaaagg agaagctcaa ctcaagccca 300agagctttgc taaggcccta acaagcccac caaagcaaaa agcccactgg ctcacgctag 360gaaccaaaag gcccagcagt gatccagccc caaaagagat ctcctttgcc ccggagatta 420caatggacga tttcctctat ctttacgatc taggaaggaa gttcgaaggt gaaggtgacg 480acactatgtt caccactgat aatgagaagg ttagcctctt caatttcaga aagaatgctg 540acccacagat ggttagagag gcctacgcag caggtctcat caagacgatc tacccgagta 600acaatctcca ggagatcaaa taccttccca agaaggttaa agatgcagtc aaaagattca 660ggactaattg catcaagaac acagagaaag acatatttct caagatcaga agtactattc 720cagtatggac gattcaaggc ttgcttcata aaccaaggca agtaatagag attggagtct 780ctaaaaaggt agttcctact gaatctaagg ccatgcatgg agtctaagat tcaaatcgag 840gatctaacag aactcgccgt gaagactggc gaacagttca tacagagtct tttacgactc 900aatgacaaga agaaaatctt cgtcaacatg gtggagcacg acactctggt ctactccaaa 960aatgtcaaag atacagtctc agaagaccaa agggctattg agacttttca acaaaggata 1020atttcgggaa acctcctcgg attccattgc ccagctatct gtcacttcat cgaaaggaca 1080gtagaaaagg aaggtggctc ctacaaatgc catcattgcg ataaaggaaa ggctatcatt 1140caagatctct ctgccgacag tggtcccaaa gatggacccc cacccacgag gagcatcgtg 1200gaaaaagaag acgttccaac cacgtcttca aagcaagtgg attgatgtga catctccact 1260gacgtaaggg atgacgcaca atcccactat ccttcgcaag acccttcctc tatataagga 1320agttcatttc atttggagag gacacgctcg aggaattcgg taccccatca caagtttgta 1380caaaaaagca ggctccgcgg ccgcttgctc cgttaaaaaa aaccatggca gagcactacg 1440ggcagcagca acaaacacgt gccccccact tgcaactgca accgcgtgct cagcgtgttg 1500taaaggcagc gaccgcggtt actgccggag gtagcctgtt ggtgttatcc gggttgaccc 1560tggctggaac ggtcattgcg ctgacaatcg ccacacctct cctggtgatc ttctcgcctg 1620tactggtccc tgcaggtaaa tttctgtgtt ccttattctc tcaaaatctt cgattttgtt 1680ttcgttcgat cccaatttcg tatatgttct ttggtttaga ttctgttaat cttagatcga 1740agacgatttt ctgggtttga tcgttagata tcatcttaat tctcgattag ggtttcatag 1800atatcatccg atttgttcaa ataatttgag ttttgtcgaa taattactct tcgatttgtg 1860atttctatct agatctggtg ttagtttcta gtttgtgcga tcgaatttgt cgattaatct 1920gagtttttct gatctgcagt catcaccatc ttcctgttgg gagcgggttt tctggcaagc 1980gggggatttg gtgttgccgc tctgtctgtg ctgtcctgga tctaccgtta cctgacgggg 2040aaacatccac ccggagcgga tcagttggag tcggccaaga caaagttggc gagcaaggcc 2100cgtgaaatga aggaccgtgc cgagcagttc agtcagcaac cggtagcagg gtctcagacc 2160agcatcgatc catcctcctg gctcgagtaa tgaagcggcc gcacccagct ttcttgtaca 2220aagtggt 2227653133DNAArtificial SequenceSynthetic sequence 65tcgacgaatt aattccaatc ccacaaaaat ctgagcttaa cagcacagtt gctcctctca 60gagcagaatc gggtattcaa caccctcata tcaactacta cgttgtgtat aacggtccac 120atgccggtat atacgatgac tggggttgta caaaggcggc aacaaacggc gttcccggag 180ttgcacacaa gaaatttgcc actattacag aggcaagagc agcagctgac gcgtacacaa 240caagtcagca aacagacagg ttgaacttca tccccaaagg agaagctcaa ctcaagccca 300agagctttgc taaggcccta acaagcccac caaagcaaaa agcccactgg ctcacgctag 360gaaccaaaag gcccagcagt gatccagccc caaaagagat ctcctttgcc ccggagatta 420caatggacga tttcctctat ctttacgatc taggaaggaa gttcgaaggt gaaggtgacg 480acactatgtt caccactgat aatgagaagg ttagcctctt caatttcaga aagaatgctg 540acccacagat ggttagagag gcctacgcag caggtctcat caagacgatc tacccgagta 600acaatctcca ggagatcaaa taccttccca agaaggttaa agatgcagtc aaaagattca 660ggactaattg catcaagaac acagagaaag acatatttct caagatcaga agtactattc 720cagtatggac gattcaaggc ttgcttcata aaccaaggca agtaatagag attggagtct 780ctaaaaaggt agttcctact gaatctaagg ccatgcatgg agtctaagat tcaaatcgag 840gatctaacag aactcgccgt gaagactggc gaacagttca tacagagtct tttacgactc 900aatgacaaga agaaaatctt cgtcaacatg gtggagcacg acactctggt ctactccaaa 960aatgtcaaag atacagtctc agaagaccaa agggctattg agacttttca acaaaggata 1020atttcgggaa acctcctcgg attccattgc ccagctatct gtcacttcat cgaaaggaca 1080gtagaaaagg aaggtggctc ctacaaatgc catcattgcg ataaaggaaa ggctatcatt 1140caagatctct ctgccgacag tggtcccaaa gatggacccc cacccacgag gagcatcgtg 1200gaaaaagaag acgttccaac cacgtcttca aagcaagtgg attgatgtga catctccact 1260gacgtaaggg atgacgcaca atcccactat ccttcgcaag acccttcctc tatataagga 1320agttcatttc atttggagag gacacgctcg aggaattcgg taccccatca caagtttgta 1380caaaaaagca ggctccgcgg ccgcttgctc cgttaaaaaa aaccatggca gagcactacg 1440ggcagcagca acaaacacgt gccccccact tgcaactgca accgcgtgct cagcgtgttg 1500taaaggcagc gaccgcggtt actgccggag gtagcctgtt ggtgttatcc gggttgaccc 1560tggctggaac ggtcattgcg ctgacaatcg ccacacctct cctggtgatc ttctcgcctg 1620tactggtccc tgcaggtaaa tttctgtgtt ccttattctc tcaaaatctt cgattttgtt 1680ttcgttcgat cccaatttcg tatatgttct ttggtttaga ttctgttaat cttagatcga 1740agacgatttt ctgggtttga tcgttagata tcatcttaat tctcgattag ggtttcatag 1800atatcatccg atttgttcaa ataatttgag ttttgtcgaa taattactct tcgatttgtg 1860atttctatct agatctggtg ttagtttcta gtttgtgcga tcgaatttgt cgattaatct 1920gagtttttct gatctgcagt catcaccatc ttcctgttgg gagcgggttt tctggcaagc 1980gggggatttg gtgttgccgc tctgtctgtg ctgtcctgga tctaccgtta cctgacgggg 2040aaacatccac ccggagcgga tcagttggag tcggccaaga caaagttggc gagcaaggcc 2100cgtgaaatga aggaccgtgc cgagcagttc agtcagcaac cggtagcagg gtctcagacc 2160agcatcgatc catcctcctg gcatatgatg gccgagcact atggacaaca gcagcagacg 2220cgtgcccctc atctgcaact gcaaccccgt gctcaacgtg tcgttaaggc tgcgacagca 2280gtaaccgctg ggggttctct gttagtgttg tcagggctga ctttggcggg gacggtaatt 2340gcgttgacca ttgccacccc gctgttagtg attttcagcc cggtactggt gccagcagtt 2400atcacgatct tcttgctggg tgccggattc ttggcaagtg gaggttttgg agttgcggcg 2460ctgtcagttt tatcctggat ctatcgttat ctgacaggaa aacatccccc aggtgccgat 2520cagctggaga gtgccaagac aaaactggcg tctaaggcac gtgaaatgaa ggatcgtgcc 2580gaacagtttt ctcaacagcc cgtagcgggg tcacagacct cgatcgatca gcaggttaac 2640gtgcacatgg ccgaacatta cggacagcaa caacagacgc gtgctccaca cctgcaattg 2700caaccgcgtg ctcaacgtgt tgtcaaagcg gcgaccgccg taacagcagg aggatcactg 2760ttagtgctgt cgggtttaac cttggccggg accgtcattg cattgactat tgcgacgccc 2820ttactggtga tcttttctcc ggtgctggtt cccgccgtta ttaccatctt cttgttaggg 2880gcaggattcc tggcatcagg gggattcgga gttgcggcgt tgagtgtctt aagttggatc 2940taccgttatc tgactggaaa gcacccgcct ggggccgatc aactggagtc agccaaaacg 3000aaattggcgt caaaagcgcg tgaaatgaag gaccgtgctg agcagttttc tcagcagcct 3060gtggcaggat cccagacatc accatggctc gagtaatgaa gcggccgcac ccagctttct 3120tgtacaaagt ggt 3133663610DNAArtificial SequenceSynthetic sequence 66tcgacgaatt aattccaatc ccacaaaaat ctgagcttaa cagcacagtt gctcctctca 60gagcagaatc gggtattcaa caccctcata tcaactacta cgttgtgtat aacggtccac 120atgccggtat atacgatgac tggggttgta caaaggcggc aacaaacggc gttcccggag 180ttgcacacaa gaaatttgcc actattacag aggcaagagc agcagctgac gcgtacacaa 240caagtcagca aacagacagg ttgaacttca tccccaaagg agaagctcaa ctcaagccca 300agagctttgc taaggcccta acaagcccac caaagcaaaa agcccactgg ctcacgctag 360gaaccaaaag gcccagcagt gatccagccc caaaagagat ctcctttgcc ccggagatta 420caatggacga tttcctctat ctttacgatc taggaaggaa gttcgaaggt gaaggtgacg 480acactatgtt caccactgat aatgagaagg ttagcctctt caatttcaga aagaatgctg 540acccacagat ggttagagag gcctacgcag caggtctcat caagacgatc tacccgagta 600acaatctcca ggagatcaaa taccttccca agaaggttaa agatgcagtc aaaagattca 660ggactaattg catcaagaac acagagaaag acatatttct caagatcaga agtactattc 720cagtatggac gattcaaggc ttgcttcata aaccaaggca agtaatagag attggagtct 780ctaaaaaggt agttcctact gaatctaagg ccatgcatgg agtctaagat tcaaatcgag 840gatctaacag aactcgccgt gaagactggc gaacagttca tacagagtct tttacgactc 900aatgacaaga agaaaatctt cgtcaacatg gtggagcacg acactctggt ctactccaaa 960aatgtcaaag atacagtctc agaagaccaa agggctattg agacttttca acaaaggata 1020atttcgggaa acctcctcgg attccattgc ccagctatct gtcacttcat cgaaaggaca 1080gtagaaaagg aaggtggctc ctacaaatgc catcattgcg ataaaggaaa ggctatcatt 1140caagatctct ctgccgacag tggtcccaaa gatggacccc cacccacgag gagcatcgtg 1200gaaaaagaag acgttccaac cacgtcttca aagcaagtgg attgatgtga catctccact 1260gacgtaaggg atgacgcaca atcccactat ccttcgcaag acccttcctc tatataagga 1320agttcatttc atttggagag gacacgctcg aggaattcgg taccccatca caagtttgta 1380caaaaaagca ggctccgcgg ccgcttgctc cgttaaaaaa aaccatggca gagcactacg 1440ggcagcagca acaaacacgt gccccccact tgcaactgca accgcgtgct cagcgtgttg 1500taaaggcagc gaccgcggtt actgccggag gtagcctgtt ggtgttatcc gggttgaccc 1560tggctggaac ggtcattgcg ctgacaatcg ccacacctct cctggtgatc ttctcgcctg 1620tactggtccc tgcaggtaaa tttctgtgtt ccttattctc tcaaaatctt cgattttgtt 1680ttcgttcgat cccaatttcg tatatgttct ttggtttaga ttctgttaat cttagatcga 1740agacgatttt ctgggtttga tcgttagata tcatcttaat tctcgattag ggtttcatag 1800atatcatccg atttgttcaa ataatttgag ttttgtcgaa taattactct tcgatttgtg 1860atttctatct agatctggtg ttagtttcta gtttgtgcga tcgaatttgt cgattaatct 1920gagtttttct gatctgcagt catcaccatc ttcctgttgg gagcgggttt tctggcaagc 1980gggggatttg gtgttgccgc tctgtctgtg ctgtcctgga tctaccgtta cctgacgggg 2040aaacatccac ccggagcgga tcagttggag tcggccaaga caaagttggc gagcaaggcc 2100cgtgaaatga aggaccgtgc cgagcagttc agtcagcaac cggtagcagg gtctcagacc 2160agcatcgatc catcctcctg gctcgagatg gcggaacact acgggcaaca acagcagact 2220cgtgctcccc acctgcaatt acaaccccgt gcccaacgtg ttgtgaaagc ggcaacagca 2280gtaacggcag ggggaagttt gctggtctta tcggggttga ccttagcggg aaccgtgatt 2340gccctgacaa ttgcgactcc gctgctggtt atcttcagcc ccgtattggt tccggccgtg 2400atcacgattt ttttgctggg ggcaggattt ttagccagcg gaggatttgg ggtcgcagcg 2460ttgtctgtgc tgagttggat ctatcgttat ttgaccggga agcacccacc tggagcagac 2520cagctggaga gcgcgaaaac gaagctggca tcgaaggcgc gtgaaatgaa ggatcgtgct 2580gaacaattct cccagcagcc tgttgccggt tctcagacca gccatatgat ggccgagcac 2640tatggacaac agcagcagac gcgtgcccct catctgcaac tgcaaccccg tgctcaacgt 2700gtcgttaagg ctgcgacagc agtaaccgct gggggttctc tgttagtgtt gtcagggctg 2760actttggcgg ggacggtaat tgcgttgacc attgccaccc cgctgttagt gattttcagc 2820ccggtactgg tgccagcagt tatcacgatc ttcttgctgg gtgccggatt cttggcaagt 2880ggaggttttg gagttgcggc gctgtcagtt ttatcctgga tctatcgtta tctgacagga 2940aaacatcccc caggtgccga tcagctggag agtgccaaga caaaactggc gtctaaggca 3000cgtgaaatga aggatcgtgc cgaacagttt tctcaacagc ccgtagcggg gtcacagacc 3060tcgatcgatc agcaggttaa cgtgcacatg gccgaacatt acggacagca acaacagacg 3120cgtgctccac acctgcaatt gcaaccgcgt gctcaacgtg ttgtcaaagc ggcgaccgcc 3180gtaacagcag gaggatcact gttagtgctg tcgggtttaa ccttggccgg gaccgtcatt 3240gcattgacta ttgcgacgcc cttactggtg atcttttctc cggtgctggt tcccgccgtt 3300attaccatct tcttgttagg ggcaggattc ctggcatcag ggggattcgg agttgcggcg 3360ttgagtgtct taagttggat ctaccgttat ctgactggaa agcacccgcc tggggccgat 3420caactggagt cagccaaaac gaaattggcg tcaaaagcgc gtgaaatgaa ggaccgtgct 3480gagcagtttt ctcagcagcc tgtggcagga tcccagacat caccatggct cgagtaatga 3540agcggccgca cccagctttc ttgtacaaag tggtgatggg ttcgaaatcg ataagcttgg 3600atcctctaga 3610674510DNAArtificial SequenceSynthetic sequence 67tcgacgaatt aattccaatc ccacaaaaat ctgagcttaa cagcacagtt gctcctctca 60gagcagaatc gggtattcaa caccctcata tcaactacta cgttgtgtat aacggtccac 120atgccggtat atacgatgac tggggttgta caaaggcggc aacaaacggc gttcccggag 180ttgcacacaa gaaatttgcc actattacag aggcaagagc agcagctgac gcgtacacaa 240caagtcagca aacagacagg ttgaacttca tccccaaagg agaagctcaa ctcaagccca 300agagctttgc taaggcccta acaagcccac caaagcaaaa agcccactgg ctcacgctag 360gaaccaaaag gcccagcagt gatccagccc caaaagagat ctcctttgcc ccggagatta 420caatggacga tttcctctat ctttacgatc taggaaggaa gttcgaaggt gaaggtgacg 480acactatgtt caccactgat aatgagaagg ttagcctctt caatttcaga aagaatgctg 540acccacagat ggttagagag gcctacgcag caggtctcat caagacgatc tacccgagta 600acaatctcca ggagatcaaa taccttccca agaaggttaa agatgcagtc aaaagattca 660ggactaattg catcaagaac acagagaaag acatatttct caagatcaga agtactattc 720cagtatggac gattcaaggc ttgcttcata aaccaaggca agtaatagag attggagtct 780ctaaaaaggt agttcctact gaatctaagg ccatgcatgg agtctaagat tcaaatcgag 840gatctaacag aactcgccgt gaagactggc gaacagttca tacagagtct tttacgactc 900aatgacaaga agaaaatctt cgtcaacatg gtggagcacg acactctggt ctactccaaa 960aatgtcaaag atacagtctc agaagaccaa agggctattg agacttttca acaaaggata 1020atttcgggaa acctcctcgg attccattgc ccagctatct gtcacttcat cgaaaggaca 1080gtagaaaagg aaggtggctc ctacaaatgc catcattgcg ataaaggaaa ggctatcatt 1140caagatctct ctgccgacag tggtcccaaa gatggacccc cacccacgag gagcatcgtg 1200gaaaaagaag acgttccaac cacgtcttca aagcaagtgg attgatgtga catctccact 1260gacgtaaggg atgacgcaca atcccactat ccttcgcaag acccttcctc tatataagga 1320agttcatttc atttggagag gacacgctcg aggaattcgg taccccatca caagtttgta 1380caaaaaagca ggctccgcgg ccgcttgctc cgttaaaaaa aaccatggca gagcactacg 1440ggcagcagca acaaacacgt gccccccact tgcaactgca accgcgtgct cagcgtgttg 1500taaaggcagc gaccgcggtt actgccggag gtagcctgtt ggtgttatcc gggttgaccc 1560tggctggaac ggtcattgcg ctgacaatcg ccacacctct cctggtgatc ttctcgcctg 1620tactggtccc tgcaggtaaa tttctgtgtt ccttattctc tcaaaatctt cgattttgtt 1680ttcgttcgat cccaatttcg tatatgttct ttggtttaga ttctgttaat cttagatcga 1740agacgatttt ctgggtttga tcgttagata tcatcttaat tctcgattag ggtttcatag 1800atatcatccg atttgttcaa ataatttgag ttttgtcgaa taattactct tcgatttgtg 1860atttctatct agatctggtg ttagtttcta gtttgtgcga tcgaatttgt cgattaatct 1920gagtttttct gatctgcagt catcaccatc ttcctgttgg gagcgggttt tctggcaagc 1980gggggatttg gtgttgccgc tctgtctgtg ctgtcctgga tctaccgtta cctgacgggg 2040aaacatccac ccggagcgga tcagttggag tcggccaaga caaagttggc gagcaaggcc 2100cgtgaaatga aggaccgtgc cgagcagttc agtcagcaac cggtagcagg gtctcagacc 2160agcatcgatc catcctcctg gctcgagatg gcggaacact acgggcaaca acagcagact 2220cgtgctcccc acctgcaatt acaaccccgt gcccaacgtg ttgtgaaagc ggcaacagca 2280gtaacggcag ggggaagttt gctggtctta tcggggttga ccttagcggg aaccgtgatt 2340gccctgacaa ttgcgactcc gctgctggtt atcttcagcc ccgtattggt tccggccgtg 2400atcacgattt ttttgctggg ggcaggattt ttagccagcg gaggatttgg ggtcgcagcg 2460ttgtctgtgc tgagttggat ctatcgttat ttgaccggga agcacccacc tggagcagac 2520cagctggaga gcgcgaaaac gaagctggca tcgaaggcgc gtgaaatgaa ggatcgtgct 2580gaacaattct cccagcagcc tgttgccggt tctcagacca gccatatgtt taaatggcca 2640agcgctatgg ccgagcatta tgggcagcaa cagcaaaccc gtgccccgca tctgcaattg 2700caacctcgtg cccagcgtgt cgttaaggcg gctactgcgg taacagcggg agggagctta 2760ctggtattaa gcgggctgac attggccgga acggtgatcg ccttaacaat cgcgacaccc 2820ttgctggtca tcttcagtcc ggttctggtg cccgcggtga ttacgatttt cctgctggga 2880gccggtttct tagcatcggg gggttttggg gtagcagcct tgagtgtcct gtcgtggatc 2940tatcgttact taactggaaa acacccgcca ggagctgacc agttggagtc tgcaaaaact 3000aagctggcgt ccaaagcccg tgaaatgaag gatcgtgctg agcagtttag ccagcagcca 3060gttgcgggaa gtcagacctc ttcatctgag ctcccatggg tcgacatggc ggagcattac 3120ggtcaacagc aacagacccg tgctccgcac ttacaattgc aaccacgtgc tcaacgtgtc 3180gtaaaagccg ccacggcagt tactgcgggg ggatcattgc tggtgttaag tgggttgaca 3240ctggcgggga cagttattgc actgacgatc gcgaccccct tgttagtgat cttctccccc 3300gttctggttc cggcggtcat tacaatcttt ctgttgggtg ccggattttt agcctctggg 3360ggatttggag tagctgccct gtcagtgttg agctggatct accgttactt aacagggaag 3420caccctcccg gggcagatca gttggaaagc gccaagacca agctggcaag taaagcgcgt 3480gaaatgaagg accgtgccga acaattttcg cagcaaccgg ttgcgggatc acagacctct 3540agtactccat cctcctggca tatgatggcc gagcactatg gacaacagca gcagacgcgt 3600gcccctcatc tgcaactgca accccgtgct caacgtgtcg ttaaggctgc gacagcagta 3660accgctgggg gttctctgtt agtgttgtca gggctgactt tggcggggac ggtaattgcg 3720ttgaccattg ccaccccgct gttagtgatt ttcagcccgg tactggtgcc agcagttatc 3780acgatcttct tgctgggtgc cggattcttg gcaagtggag gttttggagt tgcggcgctg 3840tcagttttat cctggatcta tcgttatctg acaggaaaac atcccccagg tgccgatcag 3900ctggagagtg ccaagacaaa actggcgtct aaggcacgtg aaatgaagga tcgtgccgaa 3960cagttttctc aacagcccgt agcggggtca cagacctcga tcgatcagca ggttaacgtg 4020cacatggccg aacattacgg acagcaacaa cagacgcgtg ctccacacct gcaattgcaa 4080ccgcgtgctc aacgtgttgt caaagcggcg accgccgtaa cagcaggagg atcactgtta 4140gtgctgtcgg gtttaacctt ggccgggacc gtcattgcat tgactattgc gacgccctta 4200ctggtgatct tttctccggt gctggttccc gccgttatta ccatcttctt gttaggggca 4260ggattcctgg catcaggggg attcggagtt gcggcgttga gtgtcttaag ttggatctac 4320cgttatctga ctggaaagca cccgcctggg gccgatcaac tggagtcagc caaaacgaaa 4380ttggcgtcaa aagcgcgtga aatgaaggac cgtgctgagc agttttctca gcagcctgtg 4440gcaggatccc agacatcacc atggctcgag taatgaagcg gccgcaccca gctttcttgt 4500acaaagtggt 4510681706DNAArtificial SequenceSynthetic sequence 68gcaggaactc tctggtaagc tagctccact ccccagaaac aaccggcgcc aaattgcgcg 60aattgctgac ctgaagacgg aacatcatcg tcgggtcctt gggcgattgc ggcggaagat 120gggtcagctt gggcttgagg acgagacccg aatccgagtc tgttgaaaag gttgttcatt 180ggggatttgt atacggagat tggtcgtcga gaggtttgag ggaaaggaca aatgggtttg 240gctctggaga aagagagtgc ggctttagag agagaattga gaggtttaga gagagatgcg 300gcggcgatga gcggaggaga gacgacgagg acctgcatta tcaaagcagt gacgtggtga 360aatttggaac ttttaagagg cagatagatt tattatttgt atccattttc ttcattgttc 420tagaatgtcg cggaacaaat tttaaaacta aatcctaaat ttttctaatt ttgttgccaa 480tagtggatat gtgggccgta tagaaggaat ctattgaagg cccaaaccca tactgacgag 540cccaaaggtt cgttttgcgt tttatgtttc ggttcgatgc caacgccaca ttctgagcta 600ggcaaaaaac aaacgtgtct ttgaatagac tcctctcgtt aacacatgca gcggctgcat 660ggtgacgcca ttaacacgtg gcctacaatt gcatgatgtc tccattgaca cgtgacttct 720cgtctccttt cttaatatat ctaacaaaca ctcctacctc ttccaaaata tatacacatc 780tttttgatca atctctcatt caaaatctca ttctctctag taaacaagaa caaaaaaggt 840accccatcac aagtttgtac aaaaaagcag gctccgcggc cgcttgctcc gttaaaaaaa 900accatggcag agcactacgg gcagcagcaa caaacacgtg ccccccactt gcaactgcaa 960ccgcgtgctc

agcgtgttgt aaaggcagcg accgcggtta ctgccggagg tagcctgttg 1020gtgttatccg ggttgaccct ggctggaacg gtcattgcgc tgacaatcgc cacacctctc 1080ctggtgatct tctcgcctgt actggtccct gcaggtaaat ttctgtgttc cttattctct 1140caaaatcttc gattttgttt tcgttcgatc ccaatttcgt atatgttctt tggtttagat 1200tctgttaatc ttagatcgaa gacgattttc tgggtttgat cgttagatat catcttaatt 1260ctcgattagg gtttcataga tatcatccga tttgttcaaa taatttgagt tttgtcgaat 1320aattactctt cgatttgtga tttctatcta gatctggtgt tagtttctag tttgtgcgat 1380cgaatttgtc gattaatctg agtttttctg atctgcagtc atcaccatct tcctgttggg 1440agcgggtttt ctggcaagcg ggggatttgg tgttgccgct ctgtctgtgc tgtcctggat 1500ctaccgttac ctgacgggga aacatccacc cggagcggat cagttggagt cggccaagac 1560aaagttggcg agcaaggccc gtgaaatgaa ggaccgtgcc gagcagttca gtcagcaacc 1620ggtagcaggg tctcagacca gcatcgatcc atcctcctgg ctcgagtaat gaagcggccg 1680cacccagctt tcttgtacaa agtggt 1706692612DNAArtificial SequenceSynthetic sequence 69gcaggaactc tctggtaagc tagctccact ccccagaaac aaccggcgcc aaattgcgcg 60aattgctgac ctgaagacgg aacatcatcg tcgggtcctt gggcgattgc ggcggaagat 120gggtcagctt gggcttgagg acgagacccg aatccgagtc tgttgaaaag gttgttcatt 180ggggatttgt atacggagat tggtcgtcga gaggtttgag ggaaaggaca aatgggtttg 240gctctggaga aagagagtgc ggctttagag agagaattga gaggtttaga gagagatgcg 300gcggcgatga gcggaggaga gacgacgagg acctgcatta tcaaagcagt gacgtggtga 360aatttggaac ttttaagagg cagatagatt tattatttgt atccattttc ttcattgttc 420tagaatgtcg cggaacaaat tttaaaacta aatcctaaat ttttctaatt ttgttgccaa 480tagtggatat gtgggccgta tagaaggaat ctattgaagg cccaaaccca tactgacgag 540cccaaaggtt cgttttgcgt tttatgtttc ggttcgatgc caacgccaca ttctgagcta 600ggcaaaaaac aaacgtgtct ttgaatagac tcctctcgtt aacacatgca gcggctgcat 660ggtgacgcca ttaacacgtg gcctacaatt gcatgatgtc tccattgaca cgtgacttct 720cgtctccttt cttaatatat ctaacaaaca ctcctacctc ttccaaaata tatacacatc 780tttttgatca atctctcatt caaaatctca ttctctctag taaacaagaa caaaaaaggt 840accccatcac aagtttgtac aaaaaagcag gctccgcggc cgcttgctcc gttaaaaaaa 900accatggcag agcactacgg gcagcagcaa caaacacgtg ccccccactt gcaactgcaa 960ccgcgtgctc agcgtgttgt aaaggcagcg accgcggtta ctgccggagg tagcctgttg 1020gtgttatccg ggttgaccct ggctggaacg gtcattgcgc tgacaatcgc cacacctctc 1080ctggtgatct tctcgcctgt actggtccct gcaggtaaat ttctgtgttc cttattctct 1140caaaatcttc gattttgttt tcgttcgatc ccaatttcgt atatgttctt tggtttagat 1200tctgttaatc ttagatcgaa gacgattttc tgggtttgat cgttagatat catcttaatt 1260ctcgattagg gtttcataga tatcatccga tttgttcaaa taatttgagt tttgtcgaat 1320aattactctt cgatttgtga tttctatcta gatctggtgt tagtttctag tttgtgcgat 1380cgaatttgtc gattaatctg agtttttctg atctgcagtc atcaccatct tcctgttggg 1440agcgggtttt ctggcaagcg ggggatttgg tgttgccgct ctgtctgtgc tgtcctggat 1500ctaccgttac ctgacgggga aacatccacc cggagcggat cagttggagt cggccaagac 1560aaagttggcg agcaaggccc gtgaaatgaa ggaccgtgcc gagcagttca gtcagcaacc 1620ggtagcaggg tctcagacca gcatcgatcc atcctcctgg catatgatgg ccgagcacta 1680tggacaacag cagcagacgc gtgcccctca tctgcaactg caaccccgtg ctcaacgtgt 1740cgttaaggct gcgacagcag taaccgctgg gggttctctg ttagtgttgt cagggctgac 1800tttggcgggg acggtaattg cgttgaccat tgccaccccg ctgttagtga ttttcagccc 1860ggtactggtg ccagcagtta tcacgatctt cttgctgggt gccggattct tggcaagtgg 1920aggttttgga gttgcggcgc tgtcagtttt atcctggatc tatcgttatc tgacaggaaa 1980acatccccca ggtgccgatc agctggagag tgccaagaca aaactggcgt ctaaggcacg 2040tgaaatgaag gatcgtgccg aacagttttc tcaacagccc gtagcggggt cacagacctc 2100gatcgatcag caggttaacg tgcacatggc cgaacattac ggacagcaac aacagacgcg 2160tgctccacac ctgcaattgc aaccgcgtgc tcaacgtgtt gtcaaagcgg cgaccgccgt 2220aacagcagga ggatcactgt tagtgctgtc gggtttaacc ttggccggga ccgtcattgc 2280attgactatt gcgacgccct tactggtgat cttttctccg gtgctggttc ccgccgttat 2340taccatcttc ttgttagggg caggattcct ggcatcaggg ggattcggag ttgcggcgtt 2400gagtgtctta agttggatct accgttatct gactggaaag cacccgcctg gggccgatca 2460actggagtca gccaaaacga aattggcgtc aaaagcgcgt gaaatgaagg accgtgctga 2520gcagttttct cagcagcctg tggcaggatc ccagacatca ccatggctcg agtaatgaag 2580cggccgcacc cagctttctt gtacaaagtg gt 2612703089DNAArtificial SequenceSynthetic sequence 70gcaggaactc tctggtaagc tagctccact ccccagaaac aaccggcgcc aaattgcgcg 60aattgctgac ctgaagacgg aacatcatcg tcgggtcctt gggcgattgc ggcggaagat 120gggtcagctt gggcttgagg acgagacccg aatccgagtc tgttgaaaag gttgttcatt 180ggggatttgt atacggagat tggtcgtcga gaggtttgag ggaaaggaca aatgggtttg 240gctctggaga aagagagtgc ggctttagag agagaattga gaggtttaga gagagatgcg 300gcggcgatga gcggaggaga gacgacgagg acctgcatta tcaaagcagt gacgtggtga 360aatttggaac ttttaagagg cagatagatt tattatttgt atccattttc ttcattgttc 420tagaatgtcg cggaacaaat tttaaaacta aatcctaaat ttttctaatt ttgttgccaa 480tagtggatat gtgggccgta tagaaggaat ctattgaagg cccaaaccca tactgacgag 540cccaaaggtt cgttttgcgt tttatgtttc ggttcgatgc caacgccaca ttctgagcta 600ggcaaaaaac aaacgtgtct ttgaatagac tcctctcgtt aacacatgca gcggctgcat 660ggtgacgcca ttaacacgtg gcctacaatt gcatgatgtc tccattgaca cgtgacttct 720cgtctccttt cttaatatat ctaacaaaca ctcctacctc ttccaaaata tatacacatc 780tttttgatca atctctcatt caaaatctca ttctctctag taaacaagaa caaaaaaggt 840accccatcac aagtttgtac aaaaaagcag gctccgcggc cgcttgctcc gttaaaaaaa 900accatggcag agcactacgg gcagcagcaa caaacacgtg ccccccactt gcaactgcaa 960ccgcgtgctc agcgtgttgt aaaggcagcg accgcggtta ctgccggagg tagcctgttg 1020gtgttatccg ggttgaccct ggctggaacg gtcattgcgc tgacaatcgc cacacctctc 1080ctggtgatct tctcgcctgt actggtccct gcaggtaaat ttctgtgttc cttattctct 1140caaaatcttc gattttgttt tcgttcgatc ccaatttcgt atatgttctt tggtttagat 1200tctgttaatc ttagatcgaa gacgattttc tgggtttgat cgttagatat catcttaatt 1260ctcgattagg gtttcataga tatcatccga tttgttcaaa taatttgagt tttgtcgaat 1320aattactctt cgatttgtga tttctatcta gatctggtgt tagtttctag tttgtgcgat 1380cgaatttgtc gattaatctg agtttttctg atctgcagtc atcaccatct tcctgttggg 1440agcgggtttt ctggcaagcg ggggatttgg tgttgccgct ctgtctgtgc tgtcctggat 1500ctaccgttac ctgacgggga aacatccacc cggagcggat cagttggagt cggccaagac 1560aaagttggcg agcaaggccc gtgaaatgaa ggaccgtgcc gagcagttca gtcagcaacc 1620ggtagcaggg tctcagacca gcatcgatcc atcctcctgg ctcgagatgg cggaacacta 1680cgggcaacaa cagcagactc gtgctcccca cctgcaatta caaccccgtg cccaacgtgt 1740tgtgaaagcg gcaacagcag taacggcagg gggaagtttg ctggtcttat cggggttgac 1800cttagcggga accgtgattg ccctgacaat tgcgactccg ctgctggtta tcttcagccc 1860cgtattggtt ccggccgtga tcacgatttt tttgctgggg gcaggatttt tagccagcgg 1920aggatttggg gtcgcagcgt tgtctgtgct gagttggatc tatcgttatt tgaccgggaa 1980gcacccacct ggagcagacc agctggagag cgcgaaaacg aagctggcat cgaaggcgcg 2040tgaaatgaag gatcgtgctg aacaattctc ccagcagcct gttgccggtt ctcagaccag 2100ccatatgatg gccgagcact atggacaaca gcagcagacg cgtgcccctc atctgcaact 2160gcaaccccgt gctcaacgtg tcgttaaggc tgcgacagca gtaaccgctg ggggttctct 2220gttagtgttg tcagggctga ctttggcggg gacggtaatt gcgttgacca ttgccacccc 2280gctgttagtg attttcagcc cggtactggt gccagcagtt atcacgatct tcttgctggg 2340tgccggattc ttggcaagtg gaggttttgg agttgcggcg ctgtcagttt tatcctggat 2400ctatcgttat ctgacaggaa aacatccccc aggtgccgat cagctggaga gtgccaagac 2460aaaactggcg tctaaggcac gtgaaatgaa ggatcgtgcc gaacagtttt ctcaacagcc 2520cgtagcgggg tcacagacct cgatcgatca gcaggttaac gtgcacatgg ccgaacatta 2580cggacagcaa caacagacgc gtgctccaca cctgcaattg caaccgcgtg ctcaacgtgt 2640tgtcaaagcg gcgaccgccg taacagcagg aggatcactg ttagtgctgt cgggtttaac 2700cttggccggg accgtcattg cattgactat tgcgacgccc ttactggtga tcttttctcc 2760ggtgctggtt cccgccgtta ttaccatctt cttgttaggg gcaggattcc tggcatcagg 2820gggattcgga gttgcggcgt tgagtgtctt aagttggatc taccgttatc tgactggaaa 2880gcacccgcct ggggccgatc aactggagtc agccaaaacg aaattggcgt caaaagcgcg 2940tgaaatgaag gaccgtgctg agcagttttc tcagcagcct gtggcaggat cccagacatc 3000accatggctc gagtaatgaa gcggccgcac ccagctttct tgtacaaagt ggtgatgggt 3060tcgaaatcga taagcttgga tcctctaga 3089713989DNAArtificial SequenceSynthetic sequence 71gcaggaactc tctggtaagc tagctccact ccccagaaac aaccggcgcc aaattgcgcg 60aattgctgac ctgaagacgg aacatcatcg tcgggtcctt gggcgattgc ggcggaagat 120gggtcagctt gggcttgagg acgagacccg aatccgagtc tgttgaaaag gttgttcatt 180ggggatttgt atacggagat tggtcgtcga gaggtttgag ggaaaggaca aatgggtttg 240gctctggaga aagagagtgc ggctttagag agagaattga gaggtttaga gagagatgcg 300gcggcgatga gcggaggaga gacgacgagg acctgcatta tcaaagcagt gacgtggtga 360aatttggaac ttttaagagg cagatagatt tattatttgt atccattttc ttcattgttc 420tagaatgtcg cggaacaaat tttaaaacta aatcctaaat ttttctaatt ttgttgccaa 480tagtggatat gtgggccgta tagaaggaat ctattgaagg cccaaaccca tactgacgag 540cccaaaggtt cgttttgcgt tttatgtttc ggttcgatgc caacgccaca ttctgagcta 600ggcaaaaaac aaacgtgtct ttgaatagac tcctctcgtt aacacatgca gcggctgcat 660ggtgacgcca ttaacacgtg gcctacaatt gcatgatgtc tccattgaca cgtgacttct 720cgtctccttt cttaatatat ctaacaaaca ctcctacctc ttccaaaata tatacacatc 780tttttgatca atctctcatt caaaatctca ttctctctag taaacaagaa caaaaaaggt 840accccatcac aagtttgtac aaaaaagcag gctccgcggc cgcttgctcc gttaaaaaaa 900accatggcag agcactacgg gcagcagcaa caaacacgtg ccccccactt gcaactgcaa 960ccgcgtgctc agcgtgttgt aaaggcagcg accgcggtta ctgccggagg tagcctgttg 1020gtgttatccg ggttgaccct ggctggaacg gtcattgcgc tgacaatcgc cacacctctc 1080ctggtgatct tctcgcctgt actggtccct gcaggtaaat ttctgtgttc cttattctct 1140caaaatcttc gattttgttt tcgttcgatc ccaatttcgt atatgttctt tggtttagat 1200tctgttaatc ttagatcgaa gacgattttc tgggtttgat cgttagatat catcttaatt 1260ctcgattagg gtttcataga tatcatccga tttgttcaaa taatttgagt tttgtcgaat 1320aattactctt cgatttgtga tttctatcta gatctggtgt tagtttctag tttgtgcgat 1380cgaatttgtc gattaatctg agtttttctg atctgcagtc atcaccatct tcctgttggg 1440agcgggtttt ctggcaagcg ggggatttgg tgttgccgct ctgtctgtgc tgtcctggat 1500ctaccgttac ctgacgggga aacatccacc cggagcggat cagttggagt cggccaagac 1560aaagttggcg agcaaggccc gtgaaatgaa ggaccgtgcc gagcagttca gtcagcaacc 1620ggtagcaggg tctcagacca gcatcgatcc atcctcctgg ctcgagatgg cggaacacta 1680cgggcaacaa cagcagactc gtgctcccca cctgcaatta caaccccgtg cccaacgtgt 1740tgtgaaagcg gcaacagcag taacggcagg gggaagtttg ctggtcttat cggggttgac 1800cttagcggga accgtgattg ccctgacaat tgcgactccg ctgctggtta tcttcagccc 1860cgtattggtt ccggccgtga tcacgatttt tttgctgggg gcaggatttt tagccagcgg 1920aggatttggg gtcgcagcgt tgtctgtgct gagttggatc tatcgttatt tgaccgggaa 1980gcacccacct ggagcagacc agctggagag cgcgaaaacg aagctggcat cgaaggcgcg 2040tgaaatgaag gatcgtgctg aacaattctc ccagcagcct gttgccggtt ctcagaccag 2100ccatatgttt aaatggccaa gcgctatggc cgagcattat gggcagcaac agcaaacccg 2160tgccccgcat ctgcaattgc aacctcgtgc ccagcgtgtc gttaaggcgg ctactgcggt 2220aacagcggga gggagcttac tggtattaag cgggctgaca ttggccggaa cggtgatcgc 2280cttaacaatc gcgacaccct tgctggtcat cttcagtccg gttctggtgc ccgcggtgat 2340tacgattttc ctgctgggag ccggtttctt agcatcgggg ggttttgggg tagcagcctt 2400gagtgtcctg tcgtggatct atcgttactt aactggaaaa cacccgccag gagctgacca 2460gttggagtct gcaaaaacta agctggcgtc caaagcccgt gaaatgaagg atcgtgctga 2520gcagtttagc cagcagccag ttgcgggaag tcagacctct tcatctgagc tcccatgggt 2580cgacatggcg gagcattacg gtcaacagca acagacccgt gctccgcact tacaattgca 2640accacgtgct caacgtgtcg taaaagccgc cacggcagtt actgcggggg gatcattgct 2700ggtgttaagt gggttgacac tggcggggac agttattgca ctgacgatcg cgaccccctt 2760gttagtgatc ttctcccccg ttctggttcc ggcggtcatt acaatctttc tgttgggtgc 2820cggattttta gcctctgggg gatttggagt agctgccctg tcagtgttga gctggatcta 2880ccgttactta acagggaagc accctcccgg ggcagatcag ttggaaagcg ccaagaccaa 2940gctggcaagt aaagcgcgtg aaatgaagga ccgtgccgaa caattttcgc agcaaccggt 3000tgcgggatca cagacctcta gtactccatc ctcctggcat atgatggccg agcactatgg 3060acaacagcag cagacgcgtg cccctcatct gcaactgcaa ccccgtgctc aacgtgtcgt 3120taaggctgcg acagcagtaa ccgctggggg ttctctgtta gtgttgtcag ggctgacttt 3180ggcggggacg gtaattgcgt tgaccattgc caccccgctg ttagtgattt tcagcccggt 3240actggtgcca gcagttatca cgatcttctt gctgggtgcc ggattcttgg caagtggagg 3300ttttggagtt gcggcgctgt cagttttatc ctggatctat cgttatctga caggaaaaca 3360tcccccaggt gccgatcagc tggagagtgc caagacaaaa ctggcgtcta aggcacgtga 3420aatgaaggat cgtgccgaac agttttctca acagcccgta gcggggtcac agacctcgat 3480cgatcagcag gttaacgtgc acatggccga acattacgga cagcaacaac agacgcgtgc 3540tccacacctg caattgcaac cgcgtgctca acgtgttgtc aaagcggcga ccgccgtaac 3600agcaggagga tcactgttag tgctgtcggg tttaaccttg gccgggaccg tcattgcatt 3660gactattgcg acgcccttac tggtgatctt ttctccggtg ctggttcccg ccgttattac 3720catcttcttg ttaggggcag gattcctggc atcaggggga ttcggagttg cggcgttgag 3780tgtcttaagt tggatctacc gttatctgac tggaaagcac ccgcctgggg ccgatcaact 3840ggagtcagcc aaaacgaaat tggcgtcaaa agcgcgtgaa atgaaggacc gtgctgagca 3900gttttctcag cagcctgtgg caggatccca gacatcacca tggctcgagt aatgaagcgg 3960ccgcacccag ctttcttgta caaagtggt 3989722787DNAArtificial SequenceSynthetic sequence 72tcgacgaatt aattccaatc ccacaaaaat ctgagcttaa cagcacagtt gctcctctca 60gagcagaatc gggtattcaa caccctcata tcaactacta cgttgtgtat aacggtccac 120atgccggtat atacgatgac tggggttgta caaaggcggc aacaaacggc gttcccggag 180ttgcacacaa gaaatttgcc actattacag aggcaagagc agcagctgac gcgtacacaa 240caagtcagca aacagacagg ttgaacttca tccccaaagg agaagctcaa ctcaagccca 300agagctttgc taaggcccta acaagcccac caaagcaaaa agcccactgg ctcacgctag 360gaaccaaaag gcccagcagt gatccagccc caaaagagat ctcctttgcc ccggagatta 420caatggacga tttcctctat ctttacgatc taggaaggaa gttcgaaggt gaaggtgacg 480acactatgtt caccactgat aatgagaagg ttagcctctt caatttcaga aagaatgctg 540acccacagat ggttagagag gcctacgcag caggtctcat caagacgatc tacccgagta 600acaatctcca ggagatcaaa taccttccca agaaggttaa agatgcagtc aaaagattca 660ggactaattg catcaagaac acagagaaag acatatttct caagatcaga agtactattc 720cagtatggac gattcaaggc ttgcttcata aaccaaggca agtaatagag attggagtct 780ctaaaaaggt agttcctact gaatctaagg ccatgcatgg agtctaagat tcaaatcgag 840gatctaacag aactcgccgt gaagactggc gaacagttca tacagagtct tttacgactc 900aatgacaaga agaaaatctt cgtcaacatg gtggagcacg acactctggt ctactccaaa 960aatgtcaaag atacagtctc agaagaccaa agggctattg agacttttca acaaaggata 1020atttcgggaa acctcctcgg attccattgc ccagctatct gtcacttcat cgaaaggaca 1080gtagaaaagg aaggtggctc ctacaaatgc catcattgcg ataaaggaaa ggctatcatt 1140caagatctct ctgccgacag tggtcccaaa gatggacccc cacccacgag gagcatcgtg 1200gaaaaagaag acgttccaac cacgtcttca aagcaagtgg attgatgtga catctccact 1260gacgtaaggg atgacgcaca atcccactat ccttcgcaag acccttcctc tatataagga 1320agttcatttc atttggagag gacacgctcg aggaattcgg taccccatca caagtttgta 1380caaaaaagca ggctccgcgg ccgcttgctc cgttaaaaaa aaccatggct gagcattatg 1440gtcaacaaca gcagaccagg gcgcctcacc tgcagctgca gccgcgcgcc cagcgggtag 1500tgaaggcggc caccgccgtg acagccggcg gctcgcttct cgtcctctct ggcctcactt 1560tagccggaac tgttattgcg ctcaccatcg ccactccgct gcttgtgatc tttagccccg 1620ttctggtgcc ggcggtcata accattttct tgctgggtgc gggttttctg gcatccggag 1680gcttcggcgt ggcggcgctg agtgtgctgt cgtggattta cagatatctg acagggaaac 1740acccgccggg ggcggatcag ctggaatcgg caaagacgaa gctggcgagc aaggcgcgag 1800agatgaagga tagggcagag cagttctcgc agcagcctgt tggaggcggt ggatccggag 1860gcggtggtag tatggctgag cattatggtc aacaacagca gaccagggcg cctcacctgc 1920agctgcagcc gcgcgcccag cgggtagtga aggcggccac cgccgtgaca gccggcggct 1980cgcttctcgt cctctctggc ctcactttag ccggaactgt tattgcgctc accatcgcca 2040ctccgctgct tgtgatcttt agccccgttc tggtgccggc ggtcataacc attttcttgc 2100tgggtgcggg ttttctggca tccggaggct tcggcgtggc ggcgctgagt gtgctgtcgt 2160ggatttacag atatctgaca gggaaacacc cgccgggggc ggatcagctg gaatcggcaa 2220agacgaagct ggcgagcaag gcgcgagaga tgaaggatag ggcagagcag ttctcgcagc 2280agcctgttgg gggcggtgga tccggtggag ggggatccat ggctgagcat tatggtcaac 2340aacagcagac cagggcgcct cacctgcagc tgcagccgcg cgcccagcgg gtagtgaagg 2400cggccaccgc cgtgacagcc ggcggctcgc ttctcgtcct ctctggcctc actttagccg 2460gaactgttat tgcgctcacc atcgccactc cgctgcttgt gatctttagc cccgttctgg 2520tgccggcggt cataaccatt ttcttgctgg gtgcgggttt tctggcatcc ggaggcttcg 2580gcgtggcggc gctgagtgtg ctgtcgtgga tttacagata tctgacaggg aaacacccgc 2640cgggggcgga tcagctggaa tcggcaaaga cgaagctggc gagcaaggcg cgagagatga 2700aggatagggc agagcagttc tcgcagcagc ctgttccatg gctcgagtaa tgaagcggcc 2760gcacccagct ttcttgtaca aagtggt 2787732263DNAArtificial SequenceSynthetic sequence 73gcaggaactc tctggtaagc tagctccact ccccagaaac aaccggcgcc aaattgcgcg 60aattgctgac ctgaagacgg aacatcatcg tcgggtcctt gggcgattgc ggcggaagat 120gggtcagctt gggcttgagg acgagacccg aatccgagtc tgttgaaaag gttgttcatt 180ggggatttgt atacggagat tggtcgtcga gaggtttgag ggaaaggaca aatgggtttg 240gctctggaga aagagagtgc ggctttagag agagaattga gaggtttaga gagagatgcg 300gcggcgatga gcggaggaga gacgacgagg acctgcatta tcaaagcagt gacgtggtga 360aatttggaac ttttaagagg cagatagatt tattatttgt atccattttc ttcattgttc 420tagaatgtcg cggaacaaat tttaaaacta aatcctaaat ttttctaatt ttgttgccaa 480tagtggatat gtgggccgta tagaaggaat ctattgaagg cccaaaccca tactgacgag 540cccaaaggtt cgttttgcgt tttatgtttc ggttcgatgc caacgccaca ttctgagcta 600ggcaaaaaac aaacgtgtct ttgaatagac tcctctcgtt aacacatgca gcggctgcat 660ggtgacgcca ttaacacgtg gcctacaatt gcatgatgtc tccattgaca cgtgacttct 720cgtctccttt cttaatatat ctaacaaaca ctcctacctc ttccaaaata tatacacatc 780tttttgatca atctctcatt caaaatctca ttctctctag taaacaagaa caaaaaaggt 840accccatcac aagtttgtac aaaaaagcag gctccgcggc cgcttgctcc gttaaaaaaa 900accatggctg agcattatgg tcaacaacag cagaccaggg cgcctcacct gcagctgcag 960ccgcgcgccc agcgggtagt gaaggcggcc accgccgtga cagccggcgg ctcgcttctc 1020gtcctctctg gcctcacttt agccggaact gttattgcgc tcaccatcgc cactccgctg 1080cttgtgatct ttagccccgt tctggtgccg gcggtcataa ccattttctt gctgggtgcg 1140ggttttctgg catccggagg cttcggcgtg gcggcgctga gtgtgctgtc gtggatttac 1200agatatctga cagggaaaca cccgccgggg gcggatcagc tggaatcggc aaagacgaag 1260ctggcgagca aggcgcgaga gatgaaggat agggcagagc agttctcgca gcagcctgtt 1320ggaggcggtg gatccggagg cggtggtagt atggctgagc attatggtca acaacagcag 1380accagggcgc

ctcacctgca gctgcagccg cgcgcccagc gggtagtgaa ggcggccacc 1440gccgtgacag ccggcggctc gcttctcgtc ctctctggcc tcactttagc cggaactgtt 1500attgcgctca ccatcgccac tccgctgctt gtgatcttta gccccgttct ggtgccggcg 1560gtcataacca ttttcttgct gggtgcgggt tttctggcat ccggaggctt cggcgtggcg 1620gcgctgagtg tgctgtcgtg gatttacaga tatctgacag ggaaacaccc gccgggggcg 1680gatcagctgg aatcggcaaa gacgaagctg gcgagcaagg cgcgagagat gaaggatagg 1740gcagagcagt tctcgcagca gcctgttggg ggcggtggat ccggtggagg gggatccatg 1800gctgagcatt atggtcaaca acagcagacc agggcgcctc acctgcagct gcagccgcgc 1860gcccagcggg tagtgaaggc ggccaccgcc gtgacagccg gcggctcgct tctcgtcctc 1920tctggcctca ctttagccgg aactgttatt gcgctcacca tcgccactcc gctgcttgtg 1980atctttagcc ccgttctggt gccggcggtc ataaccattt tcttgctggg tgcgggtttt 2040ctggcatccg gaggcttcgg cgtggcggcg ctgagtgtgc tgtcgtggat ttacagatat 2100ctgacaggga aacacccgcc gggggcggat cagctggaat cggcaaagac gaagctggcg 2160agcaaggcgc gagagatgaa ggatagggca gagcagttct cgcagcagcc tgttccatgg 2220ctcgagtaat gaagcggccg cacccagctt tcttgtacaa agt 226374153PRTArtificial SequenceSynthetic sequence 74Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu145 15075455PRTArtificial SequenceSynthetic sequence 75Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp His Met Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn 290 295 300Val His Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 370 375 380Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val385 390 395 400Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala 405 410 415Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 420 425 430Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 435 440 445Gln Thr Ser Pro Trp Leu Glu 450 45576602PRTArtificial SequenceSynthetic sequence 76Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Met Ala Glu His 290 295 300Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro305 310 315 320Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly 325 330 335Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala 340 345 350Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val 355 360 365Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser 370 375 380Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg385 390 395 400Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala 405 410 415Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu 420 425 430Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ile Asp Gln 435 440 445Gln Val Asn Val His Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr 450 455 460Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys465 470 475 480Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 485 490 495Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 500 505 510Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe 515 520 525Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala 530 535 540Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro545 550 555 560Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 565 570 575Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 580 585 590Ala Gly Ser Gln Thr Ser Pro Trp Leu Glu 595 60077914PRTArtificial SequenceSynthetic sequence 77Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Phe Lys Trp Pro 290 295 300Ser Ala Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 370 375 380Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val385 390 395 400Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala 405 410 415Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 420 425 430Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 435 440 445Gln Thr Ser Ser Ser Glu Leu Pro Trp Val Asp Met Ala Glu His Tyr 450 455 460Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg465 470 475 480Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 485 490 495Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu 500 505 510Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 515 520 525Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 530 535 540Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr545 550 555 560Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 565 570 575Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln 580 585 590Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ser Thr Pro Ser 595 600 605Ser Trp His Met Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 610 615 620Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala625 630 635 640Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 645 650 655Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu 660 665 670Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu 675 680 685Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 690 695 700Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro705 710 715 720Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 725 730 735Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala 740 745 750Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn Val His Met Ala Glu 755 760 765His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln 770 775 780Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly785 790 795 800Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile 805 810 815Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu 820 825 830Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala 835 840 845Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr 850 855 860Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser865 870 875 880Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala 885 890 895Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Pro Trp 900 905 910Leu Glu78153PRTArtificial SequenceSynthetic sequence 78Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu145 15079455PRTArtificial SequenceSynthetic sequence 79Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5

10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp His Met Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn 290 295 300Val His Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 370 375 380Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val385 390 395 400Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala 405 410 415Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 420 425 430Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 435 440 445Gln Thr Ser Pro Trp Leu Glu 450 45580602PRTArtificial SequenceSynthetic sequence 80Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Met Ala Glu His 290 295 300Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro305 310 315 320Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly 325 330 335Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala 340 345 350Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val 355 360 365Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser 370 375 380Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg385 390 395 400Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala 405 410 415Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu 420 425 430Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ile Asp Gln 435 440 445Gln Val Asn Val His Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr 450 455 460Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys465 470 475 480Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 485 490 495Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 500 505 510Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe 515 520 525Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala 530 535 540Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro545 550 555 560Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 565 570 575Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 580 585 590Ala Gly Ser Gln Thr Ser Pro Trp Leu Glu 595 60081914PRTArtificial SequenceSynthetic sequence 81Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr 130 135 140Ser Ile Asp Pro Ser Ser Trp Leu Glu Met Ala Glu His Tyr Gly Gln145 150 155 160Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln 165 170 175Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu 180 185 190Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile 195 200 205Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val 210 215 220Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe225 230 235 240Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr 245 250 255Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys 260 265 270Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser 275 280 285Gln Gln Pro Val Ala Gly Ser Gln Thr Ser His Met Phe Lys Trp Pro 290 295 300Ser Ala Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro305 310 315 320His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr 325 330 335Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu 340 345 350Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile 355 360 365Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly 370 375 380Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val385 390 395 400Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala 405 410 415Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu 420 425 430Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser 435 440 445Gln Thr Ser Ser Ser Glu Leu Pro Trp Val Asp Met Ala Glu His Tyr 450 455 460Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg465 470 475 480Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser 485 490 495Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu 500 505 510Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro 515 520 525Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly 530 535 540Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr545 550 555 560Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys 565 570 575Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln 580 585 590Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Ser Thr Pro Ser 595 600 605Ser Trp His Met Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg 610 615 620Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala625 630 635 640Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu 645 650 655Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu 660 665 670Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu 675 680 685Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu 690 695 700Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro705 710 715 720Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala 725 730 735Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Ala 740 745 750Gly Ser Gln Thr Ser Ile Asp Gln Gln Val Asn Val His Met Ala Glu 755 760 765His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln 770 775 780Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly785 790 795 800Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile 805 810 815Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu 820 825 830Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala 835 840 845Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr 850 855 860Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser865 870 875 880Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala 885 890 895Glu Gln Phe Ser Gln Gln Pro Val Ala Gly Ser Gln Thr Ser Pro Trp 900 905 910Leu Glu82441PRTArtificial SequenceSynthetic sequence 82Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser 130 135 140Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr145 150 155 160Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys 165 170 175Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 180 185 190Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 195 200 205Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe 210 215 220Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala225 230 235 240Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro 245 250 255Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 260 265 270Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 275 280 285Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly 290 295 300Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala305 310 315 320Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu 325 330 335Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr 340 345 350Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala 355 360 365Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly 370 375 380Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu385 390 395 400Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr 405 410 415Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe 420 425 430Ser Gln Gln Pro Val Pro Trp Leu Glu 435 44083441PRTArtificial SequenceSynthetic sequence 83Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr Arg Ala Pro His Leu1 5 10 15Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys Ala Ala Thr Ala Val 20 25 30Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly Leu Thr Leu Ala Gly 35 40 45Thr Val Ile

Ala Leu Thr Ile Ala Thr Pro Leu Leu Val Ile Phe Ser 50 55 60Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe Leu Leu Gly Ala Gly65 70 75 80Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala Leu Ser Val Leu Ser 85 90 95Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro Pro Gly Ala Asp Gln 100 105 110Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys Ala Arg Glu Met Lys 115 120 125Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val Gly Gly Gly Gly Ser 130 135 140Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly Gln Gln Gln Gln Thr145 150 155 160Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala Gln Arg Val Val Lys 165 170 175Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu Leu Val Leu Ser Gly 180 185 190Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr Ile Ala Thr Pro Leu 195 200 205Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala Val Ile Thr Ile Phe 210 215 220Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly Phe Gly Val Ala Ala225 230 235 240Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu Thr Gly Lys His Pro 245 250 255Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr Lys Leu Ala Ser Lys 260 265 270Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe Ser Gln Gln Pro Val 275 280 285Gly Gly Gly Gly Ser Gly Gly Gly Gly Ser Met Ala Glu His Tyr Gly 290 295 300Gln Gln Gln Gln Thr Arg Ala Pro His Leu Gln Leu Gln Pro Arg Ala305 310 315 320Gln Arg Val Val Lys Ala Ala Thr Ala Val Thr Ala Gly Gly Ser Leu 325 330 335Leu Val Leu Ser Gly Leu Thr Leu Ala Gly Thr Val Ile Ala Leu Thr 340 345 350Ile Ala Thr Pro Leu Leu Val Ile Phe Ser Pro Val Leu Val Pro Ala 355 360 365Val Ile Thr Ile Phe Leu Leu Gly Ala Gly Phe Leu Ala Ser Gly Gly 370 375 380Phe Gly Val Ala Ala Leu Ser Val Leu Ser Trp Ile Tyr Arg Tyr Leu385 390 395 400Thr Gly Lys His Pro Pro Gly Ala Asp Gln Leu Glu Ser Ala Lys Thr 405 410 415Lys Leu Ala Ser Lys Ala Arg Glu Met Lys Asp Arg Ala Glu Gln Phe 420 425 430Ser Gln Gln Pro Val Pro Trp Leu Glu 435 440

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